assertion retraction graph subject predicate object datatype annotation 1 0 graph DOID:0050739 rdfs:label autosomal genetic disease xsd:string 1 0 graph DOID:0050739 oio:inSubset obo:doid#DO_MGI_slim _IRI 1 0 graph DOID:0050739 oio:id DOID:0050739 xsd:string 1 0 graph DOID:0050739 oio:hasOBONamespace disease_ontology xsd:string 1 0 graph DOID:0050739 oio:creation_date 2012-07-24T04:45:53Z xsd:string 1 0 graph DOID:0050739 oio:created_by lschriml xsd:string 1 0 graph DOID:0050739 rdfs:subClassOf DOID:0050177 _IRI 1 0 graph DOID:0050739 rdf:type owl:Class _IRI 1 0 graph DOID:0050739 IAO:0000115 A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. xsd:string "{""dce:type"":[{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007637""}],""oio:hasDbXref"":[{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:http://ghr.nlm.nih.gov/glossary=autosomaldominant""},{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:http://ghr.nlm.nih.gov/handbook/inheritance/inheritancepatterns""}]}"