Review definition of Brunner Syndrome for corrections

DiseaseOntology · Jan 9, 2025 · 06e5119 · 06e5119
1 parent 659f5e6
commit 06e5119
Showing 1 changed file with 1 addition and 1 deletion.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -37688,7 +37688,7 @@ SubClassOf(obo:DOID_0060692 ObjectSomeValuesFrom(obo:RO_0002452 obo:SYMP_0000007
 
 # Class: obo:DOID_0060693 (Brunner Syndrome)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/8211186") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/8503438") obo:IAO_0000115 obo:DOID_0060693 "An amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11."@en)
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/8211186") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/8503438") obo:IAO_0000115 obo:DOID_0060693 "An amino acid metabolic disorder characterized by recessive X-linked inheritance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060693 "ICD10CM:E70.8")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060693 "MESH:C563156")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060693 "MIM:300615")