. . . . . . . "[Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t (6; 13) (q21; q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype]. 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 . "2017-10-17T13:17:33+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .