sub:provenance {
  sub:assertion dcterms:description "[Various combinations of the keywords and MeSH terms were used to screen for potentially relevant studies, specifically 'genetic polymorphisms' or 'SNPs' or 'variation' or 'single nucleotide polymorphism' or 'polymorphism' or 'mutation' or 'variant'; 'X-ray repair cross complementing protein 1' or 'Xeroderma Pigmentosum Group D Protein' or 'X-ray repair cross complementing protein 1' or 'Xeroderma Pigmentosum Group D Protein' or 'XPD' or 'Xeroderma Pigmentosum Complementation Group D Protein' or 'ERCC2' or 'XRCC1' or 'XRCC1 DNA repair protein'; and 'Cataract' or ' Membranous Cataract' or ' Pseudoaphakia.]. 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:25873778 ;
    prov:wasDerivedFrom dgn-void:BEFREE ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:BEFREE pav:importedOn "2017-02-19"^^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 .
}