[
  {
    "assertion": 1,
    "retraction": 0,
    "graph": "graph",
    "subject": "DOID:0050736",
    "predicate": "IAO:0000115",
    "object": "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.",
    "datatype": "xsd:string",
    "annotation": "{\"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\"}]}"
  }
]