Merge branch 'main' of https://github.com/DiseaseOntology/HumanDiseaseOntology

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -52565,6 +52565,7 @@ AnnotationAssertion(oboInOwl:created_by obo:DOID_0080089 "lschriml")
 AnnotationAssertion(oboInOwl:creation_date obo:DOID_0080089 "2015-11-10T16:53:39Z")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "GARD:3884")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "MIM:160565")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "ORDO:2593")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080089 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080089 "DOID:0080089")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0080089 doid:DO_rare_slim)
@@ -59399,6 +59400,7 @@ SubClassOf(obo:DOID_0080685 obo:DOID_520)
 
 AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133946/") obo:IAO_0000115 obo:DOID_0080686 "A myopathy that is characterized by the presence of tubular aggregates in myofibrils and has_material_basis_in heterozygous mutation in the ORAI1 gene on chromosome 12q24.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080686 "MIM:615883")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080686 "ORDO:2593")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080686 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080686 "DOID:0080686")
 AnnotationAssertion(rdfs:label obo:DOID_0080686 "tubular aggregate myopathy 2")