@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:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_head { this: np:hasAssertion dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_assertion; np:hasProvenance dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_provenance; np:hasPublicationInfo dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_publicationInfo; a np:Nanopublication . dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_assertion a np:Assertion . dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_provenance a np:Provenance . dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_publicationInfo a np:PublicationInfo . } dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_assertion { miriam-gene:1312 a ncit:C16612 . lld:C0042133 a ncit:C7057 . dgn-gda:DGN526aa578976b28f55bdda118b77966f8 sio:SIO_000628 miriam-gene:1312, lld:C0042133; a sio:SIO_001122 . } dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_provenance { dgn-np:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_assertion dcterms:description "[The genetic polymorphism of rs3087869 (IVS1+2329C>T) (OR 3.200, 95% CI 1.614-6.345) and rs4680 (Val158Met) (OR 5.675, 95% CI 2.696-11.942) loci on COMT, rs1048943 (Ile462Val) (OR 4.629, 95% CI 2.216-9.672) and rs4646422 (Gly45Asp) (OR 3.240, 95% CI 1.624-6.461) loci on CYP1A1 and rs1065827 (Ala119Ser) (OR 5.635, 95% CI 2.990-10.619) locus on CYP1B1 were the risk factors to UL development and rs1056836 (Leu432Val) (OR 0.188, 95% CI 0.061-0.575) locus on CYB1B1 may be the protective factor to UL.]. 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:24777039; 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:NP1177484.RAuZyWN04YgoyBD5Px5hqjB_WOSADDF5vpEWMmfuhRgpo130_publicationInfo { this: dcterms:created "2016-05-13T12:50:39+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" . }