@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:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_head { this: np:hasAssertion dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_assertion; np:hasProvenance dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_provenance; np:hasPublicationInfo dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_assertion a np:Assertion . dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_provenance a np:Provenance . dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_assertion { miriam-gene:1789 a ncit:C16612 . lld:C0278996 a ncit:C7057 . dgn-gda:DGN597fa2c20883befcd3598e8770ce8796 sio:SIO_000628 miriam-gene:1789, lld:C0278996; a sio:SIO_001122 . } dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_provenance { dgn-np:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_assertion dcterms:description "[Our meta-analysis suggested that DNMT3B -149C/T polymorphism was associated with the risk of head and neck cancer under heterozygote comparison (OR 0.73, 95 % CI 0.59-0.90) and dominant model (OR 1.75, 95 % CI 0.62-0.92), although no evidence of association between DNMT3B -149C/T polymorphism and cancer risk was observed as we compared in the pooled analyses (homozygote comparison: OR 0.96, 95 % CI 0.86-1.09; heterozygote comparison: OR 1.07, 95 % CI 0.86-0.32; dominant model: OR 1.03, 95 % CI 0.85-1.25; recessive model: OR 0.93, 95 % CI 0.8-1.08).]. 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:25433949; 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:NP1241147.RAXTz9LQnHOwkT51Kv9P5tSR3HHsz_uogy7tw7zofhVhQ130_publicationInfo { this: dcterms:created "2016-05-13T12:51:08+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" . }