. . . . . . . "[CMC may be part of a complex clinical phenotype like in patients with deficiencies of STAT3, IL-12R?1/IL-12p40 and APS-1 or may be the only or dominant phenotypic manifestation of disease which is referred to as CMC disease.]. 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 . "2017-10-17T13:18:38+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .