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lschriml
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added ordo xrefs
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src/ontology/doid-edit.owl

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@@ -52348,6 +52348,7 @@ AnnotationAssertion(oboInOwl:created_by obo:DOID_0080089 "lschriml")
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AnnotationAssertion(oboInOwl:creation_date obo:DOID_0080089 "2015-11-10T16:53:39Z")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "GARD:3884")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "MIM:160565")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080089 "ORDO:2593")
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AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080089 "disease_ontology")
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AnnotationAssertion(oboInOwl:id obo:DOID_0080089 "DOID:0080089")
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AnnotationAssertion(oboInOwl:inSubset obo:DOID_0080089 doid:DO_rare_slim)
@@ -59182,6 +59183,7 @@ SubClassOf(obo:DOID_0080685 obo:DOID_520)
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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.")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080686 "MIM:615883")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080686 "ORDO:2593")
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AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080686 "disease_ontology")
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AnnotationAssertion(oboInOwl:id obo:DOID_0080686 "DOID:0080686")
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AnnotationAssertion(rdfs:label obo:DOID_0080686 "tubular aggregate myopathy 2")

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