@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:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_head { this: np:hasAssertion dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_assertion; np:hasProvenance dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_provenance; np:hasPublicationInfo dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_publicationInfo; a np:Nanopublication . dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_assertion a np:Assertion . dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_provenance a np:Provenance . dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_publicationInfo a np:PublicationInfo . } dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_assertion { miriam-gene:120227 a ncit:C16612 . lld:C0524910 a ncit:C7057 . dgn-gda:DGN5e044a8bc0700d86edb11a0655b5e824 sio:SIO_000628 miriam-gene:120227, lld:C0524910; a sio:SIO_001122 . } dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_provenance { dgn-np:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_assertion dcterms:description "[The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs7944926, rs12785878) genotypes and 25(OH)D3 serum levels were also apparent in patients with chronic hepatitis C. The same genotypes of these single nucleotide polymorphisms (SNPs) that are associated with reduced 25(OH)D3 serum levels were found to be associated with HCV-related HCC (P = 0.07 [OR = 1.13, 95% CI = 0.99-1.28] for CYP2R1, P = 0.007 [OR = 1.56, 95% CI = 1.12-2.15] for GC, P = 0.003 [OR = 1.42, 95% CI = 1.13-1.78] for DHCR7; ORs for risk 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:23734184; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP967228.RAK8KlL_YBEl5CcZ3MVRoZAfcg4fUNpUtu5KHHglxgQ6o130_publicationInfo { this: dcterms:created "2015-08-25T14:47:31+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" . }