Add Parkinson's disease 25 inheritance and acronym

DiseaseOntology · Nov 6, 2023 · ee5ad15 · ee5ad15
1 parent b7b1f8d
commit ee5ad15
Showing 1 changed file with 2 additions and 0 deletions.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -46633,12 +46633,14 @@ SubClassOf(obo:DOID_0070484 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/36073231/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/37046398/") obo:IAO_0000115 obo:DOID_0070486 "An early-onset Parkinson's disease characterized by mild to moderately impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the PTPA gene on chromosome 9q34.11.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070486 "OMIM:620482")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070486 "PARK25")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070486 "autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0070486 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0070486 "DOID:0070486")
 AnnotationAssertion(rdfs:label obo:DOID_0070486 "Parkinson's disease 25")
 AnnotationAssertion(skos:exactMatch obo:DOID_0070486 "OMIM:620482")
 SubClassOf(obo:DOID_0070486 obo:DOID_0060894)
+SubClassOf(obo:DOID_0070486 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
 # Class: obo:DOID_0080000 (muscular disease)