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Update nomenclature of cleft palate, cardiac defects, and intellectua…
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…l disability with typo correction
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csbjohnson committed Jan 9, 2025
1 parent 9e6384d commit 3603f80
Showing 1 changed file with 2 additions and 2 deletions.
4 changes: 2 additions & 2 deletions src/ontology/doid-edit.owl
Original file line number Diff line number Diff line change
Expand Up @@ -93395,7 +93395,7 @@ SubClassOf(obo:DOID_0111696 obo:DOID_0111689)
SubClassOf(obo:DOID_0111696 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
SubClassOf(obo:DOID_0111696 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003581))

# Class: obo:DOID_0111697 (cleft palate, cardiac defects, and intellectual disabillity)
# Class: obo:DOID_0111697 (cleft palate, cardiac defects, and intellectual disability)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/24678003") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/8825606") obo:IAO_0000115 obo:DOID_0111697 "A syndrome characterized by a combination of congenital heart defects, variable cleft lip/palate, short stature, microcephaly, and digital anomalies that has_material_basis_in heterozygous mutation in the MEIS2 gene on chromosome 15q14."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111697 "MESH:C563414")
Expand All @@ -93406,7 +93406,7 @@ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111697 "cardiac malformat
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111697 "cleft palate, cardiac defects, and mental retardation"@en)
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0111697 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_0111697 "DOID:0111697")
AnnotationAssertion(rdfs:label obo:DOID_0111697 "cleft palate, cardiac defects, and intellectual disabillity"@en)
AnnotationAssertion(rdfs:label obo:DOID_0111697 "cleft palate, cardiac defects, and intellectual disability"@en)
SubClassOf(obo:DOID_0111697 obo:DOID_225)
SubClassOf(obo:DOID_0111697 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))

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