@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:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_head { this: np:hasAssertion dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_assertion; np:hasProvenance dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_provenance; np:hasPublicationInfo dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_publicationInfo; a np:Nanopublication . dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_assertion a np:Assertion . dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_provenance a np:Provenance . dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_publicationInfo a np:PublicationInfo . } dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_assertion { miriam-gene:7376 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN2565626c8c2936737c9c18f8ce0208c9 sio:SIO_000628 miriam-gene:7376, lld:C0006142; a sio:SIO_001121 . } dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_provenance { dgn-np:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_assertion dcterms:description "[The present endeavour involved study on the association of the SNP rs13181 (Lys751Gln/A18911C) in the Nucleotide Excision Repair (NER) pathway gene ERCC2 (excision repair cross-complementing rodent repair deficiency, complementation group 2) with the risks of Squamous Cell Carcinomas of the Head and Neck (SCCHN) and Breast cancer using a case-control based association study among 685 (400 controls and 285 SCCHN-affected cases) and 395 (227 normal healthy female controls and 168 breast cancer cases) ethnically-matched samples, respectively from north India using Polymerase Chain Reaction followed by Restriction Fragment Length Polymorphism (PCR-RFLP) analysis.]. 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:19615095; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP483006.RAv-TstiJfBEF32a6giO5_zCjVxzCa7NSQ1uRMDDQw6lU130_publicationInfo { this: dcterms:created "2014-10-02T12:36:49+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }