dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_provenance {
  dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_assertion dct:description "[We found no association of the homozygous 1580A, 1601C, 2166A, and 3507G genotypes with increased risks of melanoma. Exploratory analyses of subgroups of melanoma patients compared to all controls indicated no association of these genotypes with increased risks for development of multiple primary melanomas (n=28), a negative family history for melanoma (n=277), melanomas in individuals with a low number of nevi (n=273), melanomas in individuals older than 55 years (n=142), and melanomas thicker than 1 mm (n=126).]. 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:15494739 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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 .
}