. . . . . . . "[These findings suggest that the two patients in a Chinese family suffering from congenital nephrogenic diabetes insipidus had a 5, 995-bp deletion and 3-bp (GAG) insertion at Xq28/deletion contained the entire AVPR2 gene and exon 22 of the C1 gene.]. 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 . "2017-10-17T13:10:48+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .