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 SPAC13A11.04c.1: ISS must have a "with=": failed to load qualifier 'aspect=F; term=RNA polymerase II general transcription initiation factor activity; GOid=GO:0016251; evidence=ISS; db_xref=GO_REF:0000051; from=GO:0000124; date=20200226' from SPAC13A11.04c.1:
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 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 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 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 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 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 SPAC6G10.09.1: can't find new term for MOGS-CDG disorder in mapping for disease_ontology: failed to load qualifier 'term=disease associated, MOGS-CDG disorder; db_xref=PMID:30389790; date=20190723' from SPAC6G10.09
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 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 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 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 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 SPBC28F2.11.1: no $cv_name at /local-homes/pbuild/git/pombase-legacy/lib/PomBase/Chado/QualifierLoad.pm line 82.: failed to load qualifier 'aspect=; term=regulation of transcription initiation from RNA polymerase I promoter; GOid=GO:1903357; evidence=ISS; db_xref=GO_REF:0000024; with=UniProtKB:P17480; date=20200224' from SPBC28F2.11.1:
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 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 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 SPBC29A10.16c.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 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 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 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 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 SPCC1393.02c.1: with value "UniProtKB:" should be in the form "DB:ACCESSION": failed to load qualifier 'aspect=P; term=nucleosome assembly; GOid=GO:0006334; evidence=ISS; db_xref=GO_REF:0000024; with=UniProtKB:; date=20200226' from SPCC1393.02c.1:
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 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 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