assertion retraction graph subject predicate object datatype annotation 1 0 graph DOID:3184 oio:inSubset obo:doid#NCIthesaurus _IRI 1 0 graph DOID:3184 rdfs:subClassOf DOID:3181 _IRI 1 0 graph DOID:3184 oio:hasDbXref SNOMEDCT_US_2023_03_01:254950006 xsd:string 1 0 graph DOID:3184 oio:hasExactSynonym Well differentiated Spinal Cord Oligodendroglioma @en 1 0 graph DOID:3184 oio:hasOBONamespace disease_ontology xsd:string 1 0 graph DOID:3184 rdf:type owl:Class _IRI 1 0 graph DOID:3184 oio:hasDbXref NCI:C4535 xsd:string 1 0 graph DOID:3184 rdfs:subClassOf DOID:3185 _IRI 1 0 graph DOID:3184 oio:id DOID:3184 xsd:string 1 0 graph DOID:5351 rdfs:label ovarian primitive germ cell tumor xsd:string 1 0 graph DOID:5351 oio:inSubset obo:doid#NCIthesaurus _IRI 1 0 graph DOID:5351 oio:id DOID:5351 xsd:string 1 0 graph DOID:5351 oio:hasOBONamespace disease_ontology xsd:string 1 0 graph DOID:5351 oio:hasDbXref UMLS_CUI:C1518727 xsd:string 1 0 graph DOID:5351 oio:hasDbXref NCI:C39986 xsd:string 1 0 graph DOID:5351 rdfs:subClassOf DOID:2155 _IRI 1 0 graph DOID:5351 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""}]}" 1 0 graph DOID:7650 rdfs:label pulmonary type ovarian small cell carcinoma xsd:string 1 0 graph DOID:7650 oio:inSubset obo:doid#NCIthesaurus _IRI