@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:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_head { this: np:hasAssertion dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_assertion; np:hasProvenance dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_provenance; np:hasPublicationInfo dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_publicationInfo; a np:Nanopublication . dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_assertion a np:Assertion . dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_provenance a np:Provenance . dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_assertion { miriam-gene:4254 a ncit:C16612 . lld:C0855197 a ncit:C7057 . dgn-gda:DGNd4731065d8ae994caa865f407a4ae698 sio:SIO_000628 miriam-gene:4254, lld:C0855197; a sio:SIO_001121 . } dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_provenance { dgn-np:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_assertion dcterms:description "[Although most variants are cancer specific, pleiotropy has been observed for several variants, for example, variants at the 8q24 locus and breast, ovarian and prostate cancers or variants in KITLG in relation to hair color and testicular cancer.]. 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:21459759; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP884138.RAdw-qWagYU0Xg8PzP8vybz2mXiD7Ll7hJwpe00AlmCoQ130_publicationInfo { this: dcterms:created "2016-05-13T12:48:25+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }