. . . . . . . "[In AQP2-affected NDI, comparison of genotype (types of mutations and mutated residues) and phenotype (clinical characteristics) provides better understanding of both clinical entity of the disease and molecular mechanisms regulating AQP2.]. 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 . "2017-10-17T13:10:41+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .