assertion  retraction  graph  subject       predicate            object                                                                                                                                                                             datatype    annotation
1          0           graph  DOID:0050737  rdfs:label           autosomal recessive disease                                                                                                                                                        xsd:string  
1          0           graph  DOID:0050737  oio:id               DOID:0050737                                                                                                                                                                       xsd:string  
1          0           graph  DOID:0050737  oio:hasOBONamespace  disease_ontology                                                                                                                                                                   xsd:string  
1          0           graph  DOID:0050737  oio:creation_date    2012-07-24T12:51:47Z                                                                                                                                                               xsd:string  
1          0           graph  DOID:0050737  oio:created_by       lschriml                                                                                                                                                                           xsd:string  
1          0           graph  DOID:0050737  rdfs:subClassOf      DOID:0050739                                                                                                                                                                       _IRI        
1          0           graph  DOID:0050737  rdf:type             owl:Class                                                                                                                                                                          _IRI        
1          0           graph  DOID:0050737  IAO:0000115          An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop.  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/handbook/inheritance/inheritancepatterns""},{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:http://www.nlm.nih.gov/medlineplus/ency/article/002052.htm""}]}"