. . . . . . . "[G?11 mutants with loss of function cause familial hypocalciuric hypercalcemia type 2, and G?11 mutants with gain of function cause a clinical disorder designated as autosomal dominant hypocalcemia type 2.]. 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 . "2017-10-17T13:13:02+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .