xref update

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -80141,7 +80141,7 @@ SubClassOf(obo:DOID_0110715 ObjectSomeValuesFrom(obo:RO_0004019 obo:HP_0001197))
 
 # Class: obo:DOID_0110716 (Warburg micro syndrome 1)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/20512159/") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20512159") obo:IAO_0000115 obo:DOID_0110716 "A Warburg micro syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severely impaired intellectual development, spastic diplegia, and hypogonadism that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/20512159/") obo:IAO_0000115 obo:DOID_0110716 "A Warburg micro syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severely impaired intellectual development, spastic diplegia, and hypogonadism that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110716 "ICD10CM:Q87.0")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110716 "MIM:600118")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110716 "Micro Syndrome 1")