Review definition of congenital dyserythropoietic anemia type Ib

Issue #1090
DiseaseOntology · Dec 30, 2024 · 69cbd20 · 69cbd20
1 parent 3d196c1
commit 69cbd20
Showing 1 changed file with 1 addition and 1 deletion.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -88654,7 +88654,7 @@ SubClassOf(obo:DOID_0111396 ObjectSomeValuesFrom(obo:RO_0004019 obo:HP_0001197))
 
 # Class: obo:DOID_0111397 (congenital dyserythropoietic anemia type Ib)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/23716552") obo:IAO_0000115 obo:DOID_0111397 "A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14."@en)
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/23716552") obo:IAO_0000115 obo:DOID_0111397 "A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the C15ORF41 gene on chromosome 15q14."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111397 "MESH:D000742")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111397 "MIM:615631")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111397 "SNOMEDCT_US_2023_03_01:59548005")