@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:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_head { this: np:hasAssertion dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_assertion; np:hasProvenance dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_provenance; np:hasPublicationInfo dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_publicationInfo; a np:Nanopublication . dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_assertion a np:Assertion . dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_provenance a np:Provenance . dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_publicationInfo a np:PublicationInfo . } dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C0268138 a ncit:C7057 . dgn-gda:DGN9cf6710fb3ed92b203162dc629d95aac sio:SIO_000628 miriam-gene:7515, lld:C0268138; a sio:SIO_001122 . } dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_provenance { dgn-np:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_assertion dcterms:description "[By using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP), we analysed XRCC1-Arg399Gln and XPD-Lys751Gln polymorphisms in 195 patients with cataract (75 patients with cortical, 53 with nuclear, 37 with posterior subcapsular, and 30 with mixed type) and in 194 otherwise healthy control group of similar age.]. 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:17637462; 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:NP620578.RAFgNomYyN6_WaYCCuhXy4dgI4C7VaBHBcWjAVf-PyaRo130_publicationInfo { this: dcterms:created "2016-05-13T12:46:27+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" . }