Correct typo in chromosome 15q11.2 deletion syndrome definition for a…

…ccuracy
DiseaseOntology · Jan 6, 2025 · 12aa422 · 12aa422
1 parent 461c42d
commit 12aa422
Showing 1 changed file with 1 addition and 1 deletion.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -34092,7 +34092,7 @@ SubClassOf(obo:DOID_0060392 obo:DOID_0060388)
 
 # Class: obo:DOID_0060393 (chromosome 15q11.2 deletion syndrome)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/615656") obo:IAO_0000115 obo:DOID_0060393 "A chromosomal deletion syndrome that is characterized by intellectual disbaility, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15."@en)
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/615656") obo:IAO_0000115 obo:DOID_0060393 "A chromosomal deletion syndrome that is characterized by intellectual disability, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15."@en)
 AnnotationAssertion(oboInOwl:created_by obo:DOID_0060393 "elvira")
 AnnotationAssertion(oboInOwl:creation_date obo:DOID_0060393 "2015-09-28T16:21:07Z")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060393 "MIM:615656")