no SO type for mRNA - skipping
  CU329670_intron_4618988..4619032 has no uniquename - skipping
  CU329670_intron_4738675..4738716 has no uniquename - skipping
  CU329670_intron_4826298..4826342 has no uniquename - skipping
can't find feature for: ATP5MPL
ortholog (ATP5MPL) not found
can't find feature for: ATP5MD
ortholog (ATP5MD) not found
can't find new term for Epilepsy, early-onset, vitamin B6-dependent in mapping for mondo: failed to load qualifier 'term=disease associated, Epilepsy, early-onset, vitamin B6-dependent; date=20180910' from SPAC644.09
can't find new term for telomere syndromes in mapping for mondo: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPNCRNA.214
unknown qualifier: /obsolete_id
can't find new term for microcephaly-capillary malformation syndrome (MICCAP) in mapping for mondo: failed to load qualifier 'term=disease associated, microcephaly-capillary malformation syndrome (MICCAP); date=20151204' from SPAC19B12.10
can't find feature for: SGD:S000029663
ortholog (SGD:S000029663) not found
can't find feature for: SGD:S000029664
ortholog (SGD:S000029664) not found
can't find feature for: SGD:S000029665
ortholog (SGD:S000029665) not found
can't find feature for: SGD:S000029662
ortholog (SGD:S000029662) not found
ignoring /systematic_id=SPBC119.04 on misc_feature
ignoring /systematic_id=SPBC17A3.07 on misc_feature
no SO type for mRNA - skipping
no SO type for mRNA - skipping
ignoring /systematic_id=SPBC19C2.05 on misc_feature
ignoring /systematic_id=SPBC19C2.05 on misc_feature
  CU329671_intron_1715443..1715483 has no uniquename - skipping
  CU329671_intron_3391070..3391177 has no uniquename - skipping
can't find new term for telomere syndromes in mapping for mondo: failed to load qualifier 'term=disease associated, telomere syndromes; date=20180407' from SPBC29A3.14c
can't find feature for: YGR169C-C
ortholog (YGR169C-C) not found
can't find new term for DNA repair-deficiency disorders in mapping for mondo: failed to load qualifier 'term=disease associated, DNA repair-deficiency disorders; date=20160105' from SPBC16A3.11
ID in EMBL file (GO:0016074) doesn't match ID in Chado (GO:0016077) for EMBL term name sno(s)RNA catabolic process   (Chado term name: sno(s)RNA metabolic process): failed to load qualifier 'aspect=P; term=sno(s)RNA catabolic process; GOid=GO:0016074; evidence=ISS; db_xref=GO_REF:0000024; with=SGD:S000001082; date=20050413' from SPCC613.07.1:
term 'MONDO:0016021' in mondo is obsolete: failed to load qualifier 'term=disease associated, encephalopathy; db_xref=PMID:24938147; date=20141024' from SPCC584.05
ID in EMBL file (GO:0017091) doesn't match ID in Chado (GO:0035925) for EMBL term name AU-rich element binding   (Chado term name: mRNA 3'-UTR AU-rich region binding): failed to load qualifier 'aspect=F; term=AU-rich element binding; GOid=GO:0017091; evidence=ISO; db_xref=GO_REF:0000024; with=SGD:S000000250; date=20070808' from SPCC1442.16c.1:
found cvterm by ID, but name doesn't match any cvterm: GO:0043144 EMBL file: snoRNA processing  Chado name for ID: sno(s)RNA processing: failed to load qualifier 'aspect=P; term=snoRNA processing; GOid=GO:0043144; evidence=ISS; db_xref=GO_REF:0000024; with=SGD:S000001123; date=20050413' from SPCC1739.07.1:
no SO type for gene - skipping
no SO type for gene - skipping
no SO type for source - skipping