@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:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_head { this: np:hasAssertion dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_assertion; np:hasProvenance dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_provenance; np:hasPublicationInfo dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_publicationInfo; a np:Nanopublication . dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_assertion a np:Assertion . dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_provenance a np:Provenance . dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_publicationInfo a np:PublicationInfo . } dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_assertion { miriam-gene:1401 a ncit:C16612 . lld:C0242383 a ncit:C7057 . dgn-gda:DGNd5c9d6ea143919c98429579692847f41 sio:SIO_000628 miriam-gene:1401, lld:C0242383; a sio:SIO_001122 . } dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_provenance { dgn-np:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_assertion dcterms:description "[Combined effects on the likelihood of early or late AMD were demonstrated for the LOC387715 Ala69Ser G/T and T/T genotypes with the markers high-sensitivity CRP (odds ratios [ORs], 1.2 for the highest tertile alone, 1.6 for G/T and T/T genotypes alone, and 2.2 for both G/T and T/T genotypes plus the highest tertile, compared with the G/G genotype with the 2 lower tertiles), IL-6 (corresponding ORs, 1.1, 1.6, and 2.2), sICAM-1 (ORs, 1.0, 1.5, and 2.3, respectively), and PAI-1 (ORs, 1.3, 1.7, and 2.3, respectively), but not with WCC, fibrinogen, homocysteine, and von Willebrand factor.]. 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:17675241; 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:NP623493.RAWAWMWSDkZgLUfdM-yVJZ6_5Kw0r8LKywcobpoU_zfyE130_publicationInfo { this: dcterms:created "2016-05-13T12:46:28+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" . }