@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_head {
  this: np:hasAssertion dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion ;
    np:hasProvenance dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion a np:Assertion .
  dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance a np:Provenance .
  dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  lld:C0086543 a ncit:C7057 .
  dgn-gda:DGN3b6abfbd9927da9140c9ec06c4ab4919 sio:SIO_000628 miriam-gene:7515 , lld:C0086543 ;
    a sio:SIO_001121 .
}
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance {
  dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_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-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}