. . . . . . . "[CGD phenotypes included both 'classic' disease with no detectable gp91-phox protein (termed X91(0)) and 'variant' phenotype with reduced but detectable gp91-phox protein (X91(-)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:11:51+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .