assertion  retraction  graph  subject       predicate    object                                                                                                                                                     datatype    annotation
1          0           graph  DOID:0050736  IAO:0000115  An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.  xsd:string  "{""dce:type"":[{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007637""},{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007640""}],""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""},{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:http://www.nlm.nih.gov/medlineplus/ency/article/002049.htm""}]}"