@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_head { this: np:hasAssertion dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_assertion; np:hasProvenance dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_provenance; np:hasPublicationInfo dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_publicationInfo; a np:Nanopublication . dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_assertion a np:Assertion . dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_provenance a np:Provenance . dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_assertion { miriam-gene:728137 a ncit:C16612 . lld:C0018206 a ncit:C7057 . dgn-gda:DGN03d9bda41aeefb47dee0bcaa10e0d81c sio:SIO_000628 miriam-gene:728137, lld:C0018206; a sio:SIO_001121 . } dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_provenance { dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_assertion dcterms:description "[Of 6 cases, 1 (16%) showed no evidence of TSPY1; in this case, which occurred in a gravida 2 para 2 woman, 2 X chromosomes were present in the nonneoplastic ovary, the gonadoblastoma, and associated dysgerminoma and granulosa cell tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:20656323; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1009513.RAgrjH31h9VVIeloYsA3QjrZbZ2DMyc7eclJti-uq5QtU130_publicationInfo { this: dcterms:created "2015-08-25T14:48:06+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }