. . . . . . . . . . . . "[A mosaic deletion of 1, 013, 395 bp in FMR1 was found (using high-density X chromosome microarray analysis followed by sequencing of the deletion breakpoints) to be the cause of Fragile X syndrome.]. 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 . "2014-10-02T12:33:21+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .