. . . . . . . "[in the Danish population, homozygosity for the HFE hemochromatosis protein C282Y mutation appears to be the prevailing cause of clinically overt genetic haemochromatosis]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:13:15+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .