Update definition and xref of X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -56044,7 +56044,7 @@ SubClassOf(obo:DOID_0080309 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0080311 (X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16158428") obo:IAO_0000115 obo:DOID_0080311 "A syndromic X-linked intellectual disability characterized by neonatal hypotonia with motor delay but no obvious ataxia, marked strabismus, early-onset complex partial seizures, and moderate to severe mental retardation and has_material_basis_in mutation in the oligophrenin-1 gene.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16158428") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/20528889/") obo:IAO_0000115 obo:DOID_0080311 "A syndromic X-linked intellectual disability characterized by moderately to severely impaired intellectual development, cerebellar hypoplasia, and seizures that has_material_basis_in mutation in the oligophrenin-1 gene on chromosome Xq12.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080311 "MIM:300486")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080311 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080311 "DOID:0080311")