mRNA SPAC18B11.05.1: can't find new term for hyperphosphatasia with mental retardation syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia with mental retardation syndrome; date=20171207' from SPAC18B11.05
mRNA SPAC18B11.05.1: can't find new term for hyperphosphatasia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia; date=20171207' from SPAC18B11.05
mRNA SPAC12G12.16c.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPAC12G12.16c
mRNA SPAC1D4.12.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPAC1D4.12
mRNA SPAC1D4.12.1: can't find new term for trichothiodystrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, trichothiodystrophy; date=20160105' from SPAC1D4.12
mRNA SPAC1687.01.1: can't find new term for ribosomopathy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, ribosomopathy; date=20171010' from SPAC1687.01
mRNA SPAC30D11.09.1: can't find new term for cerebellar atrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, cerebellar atrophy; db_xref=PMID:27016154; date=20171025' from SPAC30D11.09
mRNA SPAC56E4.06c.1: can't find new term for glutathionuria in mapping for disease_ontology: failed to load qualifier 'term=disease associated, glutathionuria; date=20060724' from SPAC56E4.06c
mRNA SPAC57A10.12c.1: can't find new term for postaxial acrofacial dysostosis syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, postaxial acrofacial dysostosis syndrome; db_xref=PMID:22692683; date=20130516' from SPAC57A10.12c
mRNA SPAC20G8.05c.1: can't find new term for PAPA syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, PAPA syndrome; date=20130320' from SPAC20G8.05c
mRNA SPAP27G11.13c.1: can't find new term for telomere syndromes in mapping for disease_ontology: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPAP27G11.13c
mRNA SPAC824.07.1: can't find new term for Paroxysmal Nonkinesigenic Dyskinesia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Paroxysmal Nonkinesigenic Dyskinesia; date=20161004' from SPAC824.07
mRNA SPAC664.09.1: can't find new term for glutathionuria in mapping for disease_ontology: failed to load qualifier 'term=disease associated, glutathionuria; date=20060724' from SPAC664.09
mRNA SPAC17A5.06.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPAC17A5.06
mRNA SPAC1002.07c.1: can't find new term for keratosis follicularis spinulosa decalvans X-linked in mapping for disease_ontology: failed to load qualifier 'term=disease associated, keratosis follicularis spinulosa decalvans X-linked; date=20170222' from SPAC1002.07c
mRNA SPAC3H1.05.1: can't find new term for progeroid disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, progeroid disorders; date=20091106' from SPAC3H1.05
mRNA SPAC4G9.09c.1: can't find new term for N-acetylglutamate synthetase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, N-acetylglutamate synthetase deficiency; date=20160106' from SPAC4G9.09c
mRNA SPAC823.07.1: can't find new term for hyperphosphatasia with mental retardation syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia with mental retardation syndrome; date=20171207' from SPAC823.07
mRNA SPAC823.07.1: can't find new term for hyperphosphatasia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia; date=20171207' from SPAC823.07
mRNA SPAC644.07.1: can't find new term for GRACILE syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, GRACILE syndrome; date=19700101' from SPAC644.07
mRNA SPAC644.07.1: can't find new term for GRACILE syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, GRACILE syndrome; date=20160106' from SPAC644.07
mRNA SPAC644.09.1: can't find new term for Epilepsy, early-onset, vitamin B6-dependent in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Epilepsy, early-onset, vitamin B6-dependent; date=20180910' from SPAC644.09
mRNA SPAC1805.02c.1: can't find new term for glutaric aciduria 2A in mapping for disease_ontology: failed to load qualifier 'term=disease associated, glutaric aciduria 2A; date=20131206' from SPAC1805.02c
mRNA SPAC3F10.04.1: can't find new term for glutathione synthetase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, glutathione synthetase deficiency; date=20160105' from SPAC3F10.04
mRNA SPAC24C9.06c.1: can't find new term for optic neuropathy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, optic neuropathy; db_xref=PMID:25351951; date=20171019' from SPAC24C9.06c
mRNA SPAC24C9.06c.1: can't find new term for cerebellar atrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, cerebellar atrophy; db_xref=PMID:25351951; date=20171019' from SPAC24C9.06c
ncRNA SPNCRNA.214.1: can't find new term for telomere syndromes in mapping for disease_ontology: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPNCRNA.214
mRNA SPAC16E8.17c.1: can't find new term for mitochondrial DNA depletion syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, mitochondrial DNA depletion syndrome; db_xref=PMID:15929042; date=20180407' from SPAC16E8.17c
mRNA SPAC4H3.08.1: can't find new term for pentosuria in mapping for disease_ontology: failed to load qualifier 'term=disease associated, pentosuria; date=20160105' from SPAC4H3.08
mRNA SPAC19G12.10c.1: can't find new term for galactosialidosis in mapping for disease_ontology: failed to load qualifier 'term=disease associated, galactosialidosis; date=20160106' from SPAC19G12.10c
mRNA SPAC1F7.03.1: ISS must have a "with=": failed to load qualifier 'aspect=F; term=mechanosensitive cation channel activity; GOid=GO:0140135; evidence=ISS; db_xref=PMID:19543678; date=20190517' from SPAC1F7.03.1:
mRNA SPAC1F7.05.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPAC1F7.05.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPAC1F7.05.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPAC1F7.05.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPAC25G10.07c.1:   unknown date format: 
mRNA SPAC27D7.06.1: can't find new term for glutaric aciduria 2A in mapping for disease_ontology: failed to load qualifier 'term=disease associated, glutaric aciduria 2A; date=20131206' from SPAC27D7.06
mRNA SPAC12B10.12c.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPAC12B10.12c
mRNA SPAC17D4.01.1: can't find new term for heredopathia atactica polyneuritiformis in mapping for disease_ontology: failed to load qualifier 'term=disease associated, heredopathia atactica polyneuritiformis; db_xref=PMID:12522768; date=20141024' from SPAC17D4.01
mRNA SPAC1782.10c.1: can't find new term for telomere syndromes in mapping for disease_ontology: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPAC1782.10c
mRNA SPAC19B12.10.1: can't find new term for microcephaly-capillary malformation syndrome (MICCAP) in mapping for disease_ontology: failed to load qualifier 'term=disease associated, microcephaly-capillary malformation syndrome (MICCAP); date=20151204' from SPAC19B12.10
mRNA SPAC29A4.04c.1: can't find new term for telomere syndromes in mapping for disease_ontology: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPAC29A4.04c
mRNA SPAC26F1.04c.1: can't find new term for childhood-onset dystonia and optic atrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, childhood-onset dystonia and optic atrophy; date=20170525' from SPAC26F1.04c
mRNA SPAC4D7.04c.1:   qualifier value ('GO_REF:0000024 with=SGD:S000000206') contains an equals '='
mRNA SPAC4D7.04c.1: ISS must have a "with=": failed to load qualifier 'aspect=C; term=endoplasmic reticulum; GOid=GO:0005783; evidence=ISS; db_xref=GO_REF:0000024 with=SGD:S000000206; date=20050414' from SPAC4D7.04c.1:
mRNA SPAC3G6.05.1: can't find new term for mitochondrial DNA depletion syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, mitochondrial DNA depletion syndrome; db_xref=PMID:15929042; date=20180407' from SPAC3G6.05
mRNA SPAC869.07c.1: can't find new term for Schindler disease in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Schindler disease; date=20160106' from SPAC869.07c
5'UTR SPBC119.04.1:5'UTR:1 from gene: SPBC119.04: ignoring /systematic_id=SPBC119.04 on misc_feature
5'UTR SPBC17A3.07.1:5'UTR:1 from gene: SPBC17A3.07: ignoring /systematic_id=SPBC17A3.07 on misc_feature
ncRNA SPNCRNA.108.1 from gene: SPNCRNA.108: ignoring /systematic_id=SPBC19C2.05 on misc_feature
CDS SPBC19C2.05.1 from gene: SPBC19C2.05: ignoring /systematic_id=SPBC19C2.05 on misc_feature
mRNA SPBC800.05c.1: can't find new term for Uner Tan syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Uner Tan syndrome; db_xref=PMID:28013290; date=20161226' from SPBC800.05c
mRNA SPBC649.03.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC649.03
mRNA SPBC577.09.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC577.09
mRNA SPBC725.14.1: can't find new term for N-acetylglutamate synthetase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, N-acetylglutamate synthetase deficiency; date=20160106' from SPBC725.14
mRNA SPBC3D6.06c.1: can't find new term for phosphoribosylpyrophosphate synthetase superactivity in mapping for disease_ontology: failed to load qualifier 'term=disease associated, phosphoribosylpyrophosphate synthetase superactivity; date=20160106' from SPBC3D6.06c
mRNA SPBC27B12.06.1: can't find new term for hyperphosphatasia with mental retardation syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia with mental retardation syndrome; date=20171207' from SPBC27B12.06
mRNA SPBC27B12.06.1: can't find new term for hyperphosphatasia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperphosphatasia; date=20171207' from SPBC27B12.06
mRNA SPBC11G11.04.1: can't find new term for X-linked spondyloepiphyseal dysplasia tarda in mapping for disease_ontology: failed to load qualifier 'term=disease associated, X-linked spondyloepiphyseal dysplasia tarda; date=19700101' from SPBC11G11.04
mRNA SPBP16F5.08c.1: can't find new term for trimethylaminuria in mapping for disease_ontology: failed to load qualifier 'term=disease associated, trimethylaminuria; date=20160106' from SPBP16F5.08c
mRNA SPBC29A3.14c.1: can't find new term for telomere syndromes in mapping for disease_ontology: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPBC29A3.14c
mRNA SPBC17G9.02c.1: can't find new term for hyperparathyroidism-jaw tumor syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperparathyroidism-jaw tumor syndrome; date=20180108' from SPBC17G9.02c
mRNA SPBC1815.01.1: can't find new term for muscle beta-enolase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, muscle beta-enolase deficiency; date=20160106' from SPBC1815.01
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000087) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000085) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000080) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000087) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000085) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000080) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000087) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000085) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000080) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000087) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000085) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC14C8.07c.1:   qualifier value ('during(GO:0000080) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC24C6.04.1: can't find new term for hyperprolinemia type 1 in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperprolinemia type 1; date=20160105' from SPBC24C6.04
mRNA SPBC19G7.01c.1: can't find new term for hereditary nonpolyposis colorectal cancer in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hereditary nonpolyposis colorectal cancer; date=20060724' from SPBC19G7.01c
mRNA SPBC29A10.01.1: can't find new term for cytochrome P450 oxidoreductase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, cytochrome P450 oxidoreductase deficiency; date=20160106' from SPBC29A10.01
mRNA SPBC29A10.05.1: can't find new term for hereditary nonpolyposis colorectal cancer in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hereditary nonpolyposis colorectal cancer; date=20070219' from SPBC29A10.05
mRNA SPBC29A10.16c.1: can't find new term for lyase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, lyase deficiency; date=20160105' from SPBC29A10.16c
mRNA SPBC3E7.08c.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC3E7.08c
mRNA SPBC336.12c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC336.12c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC336.12c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC336.12c.1:   qualifier value ('during(GO:0000089) db_xref=PMID:9755169') contains an equals '='
mRNA SPBC32F12.15.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC32F12.15
mRNA SPBC1703.04.1: can't find new term for hereditary nonpolyposis colorectal cancer in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hereditary nonpolyposis colorectal cancer; date=20060724' from SPBC1703.04
mRNA SPBC13E7.02.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC13E7.02
mRNA SPBC776.04.1: can't find new term for congenital dyserythropoietic anemia type II in mapping for disease_ontology: failed to load qualifier 'term=disease associated, congenital dyserythropoietic anemia type II; date=20151103' from SPBC776.04
mRNA SPBC11C11.02.1: can't find new term for PAPA syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, PAPA syndrome; date=20130320' from SPBC11C11.02
mRNA SPBC25D12.04.1: can't find new term for mitochondrial DNA depletion syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, mitochondrial DNA depletion syndrome; db_xref=PMID:15929042; date=20180407' from SPBC25D12.04
mRNA SPBC31F10.04c.1: can't find new term for infantile cerebral and cerebellar atrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, infantile cerebral and cerebellar atrophy; date=20101019' from SPBC31F10.04c
mRNA SPBC31F10.04c.1: can't find new term for cerebellar atrophy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, cerebellar atrophy; date=20171019' from SPBC31F10.04c
mRNA SPBC16G5.09.1: can't find new term for galactosialidosis in mapping for disease_ontology: failed to load qualifier 'term=disease associated, galactosialidosis; date=20160106' from SPBC16G5.09
mRNA SPBC16A3.15c.1: can't find new term for Uner Tan syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Uner Tan syndrome; db_xref=PMID:28013290; date=20161226' from SPBC16A3.15c
mRNA SPBC16A3.11.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC16A3.11
mRNA SPBC1289.07c.1: can't find new term for ribosomopathy in mapping for disease_ontology: failed to load qualifier 'term=disease associated, ribosomopathy; date=20171010' from SPBC1289.07c
mRNA SPCC1235.11.1: can't find new term for lactic acidosis and hyperpyruvatemia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, lactic acidosis and hyperpyruvatemia; date=20120623' from SPCC1235.11
mRNA SPCC1235.11.1: can't find new term for lactic acidosis and hyperpyruvatemia in mapping for disease_ontology: failed to load qualifier 'term=disease associated, lactic acidosis and hyperpyruvatemia; date=20120623' from SPCC1235.11
mRNA SPCC4G3.10c.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPCC4G3.10c
mRNA SPCC970.01.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPCC970.01
mRNA SPCC31H12.07.1: can't find new term for congenital dyserythropoietic anemia type II in mapping for disease_ontology: failed to load qualifier 'term=disease associated, congenital dyserythropoietic anemia type II; date=20151103' from SPCC31H12.07
mRNA SPCC16A11.10c.1: can't find new term for lyase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, lyase deficiency; date=20160105' from SPCC16A11.10c
mRNA SPCC24B10.22.1: can't find new term for mitochondrial DNA depletion syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, mitochondrial DNA depletion syndrome; db_xref=PMID:15929042; date=20180407' from SPCC24B10.22
mRNA SPCC1795.11.1: can't find new term for pediatric medulloblastoma in mapping for disease_ontology: failed to load qualifier 'term=disease associated, pediatric medulloblastoma; db_xref=PMID:25724843; date=20151013' from SPCC1795.11
mRNA SPCC4B3.03c.1: can't find new term for Jalili syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Jalili syndrome; date=20161204' from SPCC4B3.03c
mRNA SPCP25A2.02c.1: can't find new term for DNA repair-deficiency disorders in mapping for disease_ontology: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPCP25A2.02c
mRNA SPCC550.03c.1: can't find new term for trichohepatoenteric (SD/THE) syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, trichohepatoenteric (SD/THE) syndrome; date=20150520' from SPCC550.03c
mRNA SPCC18.13.1: can't find new term for microcephalic primordial dwarfism in mapping for disease_ontology: failed to load qualifier 'term=disease associated, microcephalic primordial dwarfism; db_xref=PMID:26416026; date=20160707' from SPCC18.13
mRNA SPCC18.13.1: can't find new term for Galloway-Mowat syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, Galloway-Mowat syndrome; db_xref=PMID:30079490; date=20181119' from SPCC18.13
mRNA SPCC18.18c.1: can't find new term for hereditary leiomyomatosis in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hereditary leiomyomatosis; date=20060920' from SPCC18.18c
mRNA SPCC18.18c.1: can't find new term for fumarase deficiency in mapping for disease_ontology: failed to load qualifier 'term=disease associated, fumarase deficiency; date=20160106' from SPCC18.18c
mRNA SPCC1620.08.1: can't find new term for mitochondrial DNA depletion syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, mitochondrial DNA depletion syndrome; db_xref=PMID:15929042; date=20180407' from SPCC1620.08
mRNA SPCC1919.05.1: can't find new term for trichohepatoenteric (SD/THE) syndrome in mapping for disease_ontology: failed to load qualifier 'term=disease associated, trichohepatoenteric (SD/THE) syndrome; date=20150520' from SPCC1919.05
mRNA SPCC70.03c.1: can't find new term for hyperprolinemia type 1 in mapping for disease_ontology: failed to load qualifier 'term=disease associated, hyperprolinemia type 1; date=20181126' from SPCC70.03c
mRNA SPCC1827.03c.1: can't find new term for combined malonic and methylmalonic aciduria in mapping for disease_ontology: failed to load qualifier 'term=disease associated, combined malonic and methylmalonic aciduria; date=20160106' from SPCC1827.03c
: failed to add annotation extension to SPBC14C8.07c <-> protein level: annotation extension qualifier on SPBC14C8.07c not understood: during(GO:0000080) db_xref=PMID:9755169
: failed to add annotation extension to SPBC14C8.07c <-> protein level: annotation extension qualifier on SPBC14C8.07c not understood: during(GO:0000085) db_xref=PMID:9755169
: failed to add annotation extension to SPAC1F7.05 <-> RNA level: annotation extension qualifier on SPAC1F7.05 not understood: during(GO:0000089) db_xref=PMID:9755169
: failed to add annotation extension to SPBC14C8.07c <-> protein level: annotation extension qualifier on SPBC14C8.07c not understood: during(GO:0000087) db_xref=PMID:9755169
: failed to add annotation extension to SPBC336.12c <-> RNA level: annotation extension qualifier on SPBC336.12c not understood: during(GO:0000089) db_xref=PMID:9755169
: failed to add annotation extension to SPBC14C8.07c <-> RNA level: annotation extension qualifier on SPBC14C8.07c not understood: during(GO:0000089) db_xref=PMID:9755169