@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:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_head { this: np:hasAssertion dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_assertion; np:hasProvenance dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_provenance; np:hasPublicationInfo dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_publicationInfo; a np:Nanopublication . dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_assertion a np:Assertion . dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_provenance a np:Provenance . dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_publicationInfo a np:PublicationInfo . } dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_assertion { miriam-gene:26479 a ncit:C16612 . lld:C0678222 a ncit:C7057 . dgn-gda:DGNfb114fac70faa2cbdccc42343895b042 sio:SIO_000628 miriam-gene:26479, lld:C0678222; a sio:SIO_001121 . } dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_provenance { dgn-np:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_assertion dcterms:description "[Statistically significant association with breast cancer risk was observed for rs1130409 homozygous mutant GG [odds ratio (OR) 3.35, 95% confidence interval (CI) 1.36-8.26), heterozygous GT (OR 2.42, 95% CI 1.56-3.76), and combined mutant (GT + GG) (OR 2.52, 95% CI 1.65-3.86] genotypes and rs25487 homozygous mutant AA (OR 2.91, 95% CI 1.66-5.10) and combined mutant (AA + AG) (OR 1.41, 95% CI 0.903-2.19) genotypes, whereas protective association was exhibited by rs1799782 homozygous mutant CC (OR 0.413, 95% CI 0.082-2.08), heterozygous TC (OR 0.351, 95% CI 0.189-0.650), and combined mutant (TC + CC) (OR 0.357, 95% CI 0.199-0.641) genotypes.]. 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:18669164; 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:NP876547.RApdTJZSvsoHhcky4CeNSfjDElMmx7ETdaSNwlsgGeEao130_publicationInfo { this: dcterms:created "2014-10-02T12:40:55+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" . }