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src/ontology/doid-edit.owl

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@@ -42855,9 +42855,7 @@ SubClassOf(obo:DOID_0061048 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
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# Class: obo:DOID_0061049 (autosomal dominant intellectual developmental disorder type FRA12A)
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AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/17236128/") obo:IAO_0000115 obo:DOID_0061049 "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous expanded CGG repeat in the 5-prime untranslated region of the DIP2B gene on chromosome 12q13.
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AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/17236128/") obo:IAO_0000115 obo:DOID_0061049 "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous expanded CGG repeat in the 5-prime untranslated region of the DIP2B gene on chromosome 12q13.")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061049 "MIM:136630")
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AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061049 "disease_ontology")
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AnnotationAssertion(oboInOwl:id obo:DOID_0061049 "DOID:0061049")

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