. . . . . . . "[Our observations suggest that the aberrant feed-forward pathway that keeps eIF4E and C/EBP?p30 elevated in NPM1(+/-) cells contributes to the MDS phenotype associated with NPM1 deficiency.]. 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 . "2017-10-17T13:12:16+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .