From 06e51197e1f2aa757783390183ddfca2ad3960d8 Mon Sep 17 00:00:00 2001 From: csbjohnson Date: Thu, 9 Jan 2025 18:29:21 -0500 Subject: [PATCH] Review definition of Brunner Syndrome for corrections --- src/ontology/doid-edit.owl | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl index 18b3b779..e2a71a4d 100644 --- 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")