. . . . . . . "[5% of patients with neurofibromatosis type 1 (NF1) exhibit gross deletions that encompass the NF1 gene and its flanking regions/breakpoints type 2 deletions are a second type of recurring NF1 gene deletion.]. 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 . "2017-10-17T13:14:57+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .