@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:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_head { this: np:hasAssertion dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion; np:hasProvenance dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance; np:hasPublicationInfo dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_publicationInfo; a np:Nanopublication . dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion a np:Assertion . dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance a np:Provenance . dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_publicationInfo a np:PublicationInfo . } dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C0003873 a ncit:C7057 . dgn-gda:DGN676314bd0e9a2c672c65075c279d5bcd sio:SIO_000628 miriam-gene:7515, lld:C0003873; a sio:SIO_001122 . } dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance { dgn-np:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion dcterms:description "[Although XPD (A-751G), XRCC1 (A399G), and XRCC4 (G-1394T) gene polymorphisms have been extensively investigated in different clinical pictures, this is the first study to evaluate the role of these polymorphisms in the genetic etiopathogenesis of RA in Turkish patients.]. 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:25494482; 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:NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_publicationInfo { this: dcterms:created "2016-05-13T12:51:11+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" . }