@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:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_head { this: np:hasAssertion dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_assertion; np:hasProvenance dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_provenance; np:hasPublicationInfo dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_publicationInfo; a np:Nanopublication . dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_assertion a np:Assertion . dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_provenance a np:Provenance . dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_publicationInfo a np:PublicationInfo . } dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_assertion { miriam-gene:84706 a ncit:C16612 . lld:C0015695 a ncit:C7057 . dgn-gda:DGN6f075afb6f924defd508ca6c98935be9 sio:SIO_000628 miriam-gene:84706, lld:C0015695; a sio:SIO_001122 . } dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_provenance { dgn-np:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_assertion dcterms:description "[Nine variants (rs2862954, rs1408579, rs10883451, rs11597086, rs11591741, rs17729876, rs17668255, rs17668357, rs12784396) displayed genomewide significant associations at loci concomitantly influencing FL and ALT (2.47 × 10(-9) ≤ CMA-p ≤ 4.29 × 10(-10)) as compared with the suggestive significance of marginal tests (4.11 × 10(-5) ≤ GWA-p ≤ 2.34 × 10(-6)).]. 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:23477746; 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:NP957927.RAs-0wq9Mpqpn6pTeBzJpLP2cH16dgeddCM0ghi8XYlvU130_publicationInfo { this: dcterms:created "2015-08-25T14:47:25+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" . }