Skip to content

Commit

Permalink
Fix DOID:0060999 misannotated definition & add inheritance
Browse files Browse the repository at this point in the history
  • Loading branch information
allenbaron committed Oct 31, 2024
1 parent 8d68398 commit 2527d16
Showing 1 changed file with 2 additions and 1 deletion.
3 changes: 2 additions & 1 deletion src/ontology/doid-edit.owl
Original file line number Diff line number Diff line change
Expand Up @@ -41773,12 +41773,13 @@ SubClassOf(obo:DOID_0060998 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0060999 (mitochondrial trifunctional protein deficiency 2)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12754706/") obo:IAO_0000115 obo:DOID_0060999 "A lipid metabolism disorder that has_material_basis_in homozygous or compound heterozygous mutation in the HADHB gene the beta subunit of the mitochondrial trifunctional protein, on chromosome 2p23."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060999 "MIM:620300")
AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12754706/") oboInOwl:hasOBONamespace obo:DOID_0060999 "A lipid metabolism disorder that has_material_basis_in homozygous or compound heterozygous mutation in the HADHB gene the beta subunit of the mitochondrial trifunctional protein, on chromosome 2p23.")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0060999 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_0060999 "DOID:0060999")
AnnotationAssertion(rdfs:label obo:DOID_0060999 "mitochondrial trifunctional protein deficiency 2"@en)
SubClassOf(obo:DOID_0060999 obo:DOID_3146)
SubClassOf(obo:DOID_0060999 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))

# Class: obo:DOID_0061001 (glycine encephalopathy 2)

Expand Down

0 comments on commit 2527d16

Please sign in to comment.