@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:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_head { this: np:hasAssertion dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_assertion; np:hasProvenance dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_provenance; np:hasPublicationInfo dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_publicationInfo; a np:Nanopublication . dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_assertion a np:Assertion . dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_provenance a np:Provenance . dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_publicationInfo a np:PublicationInfo . } dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_assertion { miriam-gene:356 a ncit:C16612 . lld:C0007134 a ncit:C7057 . dgn-gda:DGN60cc04e026f5686e3d61cb64f85acd17 sio:SIO_000628 miriam-gene:356, lld:C0007134; a sio:SIO_001122 . } dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_provenance { dgn-np:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_assertion dcterms:description "[In this study, we genotyped CASP8 -652 6N ins/del, FAS -1377 G > A, FAS -670 A > G, and FASL -844 C > T polymorphisms in a hospital-based case-control study of 353 patients diagnosed with RCC and 365 cancer-free controls in a Chinese population.]. 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:20572163; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP148336.RAMcmfmsizqz4HOxRWRoAD99pJXWFx3prOoq8OzeCaQdY130_publicationInfo { this: dcterms:created "2015-08-25T14:39:03+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" . }