assertion  retraction  graph  subject       predicate            object                                                                                                                  datatype    annotation
1          0           graph  DOID:0050177  IAO:0000115          A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.  xsd:string  "{""dce:type"":[{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007637""}],""oio:hasDbXref"":[{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:https://www.genome.gov/For-Patients-and-Families/Genetic-Disorders""}]}"
1          0           graph  DOID:0050177  rdfs:label           monogenic disease                                                                                                       xsd:string  
1          0           graph  DOID:0050177  oio:inSubset         obo:doid#DO_GXD_slim                                                                                                    _IRI        
1          0           graph  DOID:0050177  oio:inSubset         obo:doid#DO_AGR_slim                                                                                                    _IRI        
1          0           graph  DOID:0050177  oio:id               DOID:0050177                                                                                                            xsd:string  
1          0           graph  DOID:0050177  oio:hasOBONamespace  disease_ontology                                                                                                        xsd:string  
1          0           graph  DOID:0050177  rdfs:subClassOf      DOID:630                                                                                                                _IRI        
1          0           graph  DOID:0050177  rdf:type             owl:Class                                                                                                               _IRI