. . . . . . . "[The two main phenotypes of the MEN 2 syndrome, known as MEN 2A and MEN 2B, are associated with different mutations of the RET oncogene, mostly located on exons 10 or 11 in MEN 2A and in codon 918 of exon 16 in MEN 2B.]. 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 . "2017-10-17T13:15:57+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .