@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:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_head { this: np:hasAssertion dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_assertion; np:hasProvenance dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_provenance; np:hasPublicationInfo dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_publicationInfo; a np:Nanopublication . dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_assertion a np:Assertion . dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_provenance a np:Provenance . dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_publicationInfo a np:PublicationInfo . } dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_assertion { miriam-gene:4864 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGN594157bca791bd0c84d28f6b35b68ee6 sio:SIO_000628 miriam-gene:4864, lld:C0596263; a sio:SIO_001121 . } dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_provenance { dgn-np:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_assertion dcterms:description "[Our results indicated that mtDNA exhibited a high rate of sequence variants in patients with NPC and pedigree members and the mtDNA np16362, np16519 variants and mtMSI at D310 are associated with an increased risk of familial nasopharyngeal carcinoma in pedigree members from families with NPC, which might be involved in the NPC carcinogenesis.]. 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:21168531; 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:NP860102.RAuRLC7_SWh7X59ipikl3PsLla-6gR-IPQC_BXiXMcCxY130_publicationInfo { this: dcterms:created "2016-05-13T12:48:14+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" . }