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
ID in EMBL file (GO:0043187) doesn't match ID in Chado (GO:0000935) for EMBL term name cell septum surface   (Chado term name: division septum): failed to load qualifier 'aspect=C; term=cell septum surface; GOid=GO:0043187; evidence=IDA; db_xref=PMID:12665550; date=20040625' from SPAC821.09.1:
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
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
ISS must have a "with=": failed to load qualifier 'aspect=P; term=transcription of nuclear large rRNA transcript from RNA polymerase I promoter; qualifier=NOT; GOid=GO:0042790; evidence=ISS; db_xref=PMID:31745560; date=20200224' from SPBC14C8.14c.1:
ID in EMBL file (GO:0043187) doesn't match ID in Chado (GO:0000935) for EMBL term name cell septum surface   (Chado term name: division septum): failed to load qualifier 'aspect=C; term=cell septum surface; GOid=GO:0043187; evidence=IDA; db_xref=PMID:12356913; date=20041102' from SPBC19G7.05c.1:
can't find new term for Uner Tan syndrome in mapping for mondo: failed to load qualifier 'term=disease associated, Uner Tan syndrome; db_xref=PMID:28013290; date=20161226' from SPBC16A3.15c
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
ignoring /systematic_id=SPCC548.03c on misc_feature
can't find new term for hereditary leiomyomatosis in mapping for mondo: failed to load qualifier 'term=disease associated, hereditary leiomyomatosis; date=20060920' from SPCC18.18c
no SO type for gene - skipping
no SO type for gene - skipping
no SO type for source - skipping