. . . . . . . . . . . . "[Molecular diagnosis for cystic fibrosis (CF) is based on the direct identification of mutations in the CFTR gene cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (detection rate about 90% with scanning procedures) and on segregation analysis of intragenic polymorphisms for carrier and prenatal diagnosis in about 20% of CF families in which 1 or both causal mutations are unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2013-07-06"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:32:21+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .