. . . . . . . "[Heterozygous germline mutations of MEN1 gene are responsible for MEN1 disorders/types of mutations likely causing loss of the gene function have been identified throughout the entire region in patients with MEN1 and related disorders/.]. 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 . "2017-10-17T13:14:31+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .