dgn-np:NP1277908.RA8JRGAl5OHmNIzSN3h9EnGhH5Fpur3HF4k9oj3MwXDLY130_provenance {
  dgn-np:NP1277908.RA8JRGAl5OHmNIzSN3h9EnGhH5Fpur3HF4k9oj3MwXDLY130_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. Meta-analyses were conducted using Stata 12.0 software.]. 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-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 .
}