Update inheritance of retinitis pigmentosa 32

Issue #1090
DiseaseOntology · Jan 3, 2025 · 56b7de0 · 56b7de0
1 parent 35afc6d
commit 56b7de0
Showing 1 changed file with 1 addition and 1 deletion.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -74378,7 +74378,7 @@ SubClassOf(obo:DOID_0110354 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0110355 (retinitis pigmentosa 32)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16189710") obo:IAO_0000115 obo:DOID_0110355 "A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3."@en)
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16189710") obo:IAO_0000115 obo:DOID_0110355 "A retinitis pigmentosa that has_material_basis_inhomozygous mutation in the CLCC1 gene on chromosome 1p13."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110355 "ICD10CM:H35.5")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110355 "MESH:C563689")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110355 "MIM:609913")