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- source_evidence_literature type ECO_0000212 NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_assertion description "[It is now recognized that p53 activation, caused by haploinsufficiency for the ribosomal gene RPS14 (mapping to the commonly deleted region), is the probable cause of the erythroid defect in the 5q- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_assertion evidence source_evidence_literature NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_assertion SIO_000772 22571696 NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_assertion wasDerivedFrom befree-2016 NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_assertion wasGeneratedBy ECO_0000203 NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.
- befree-2016 importedOn "2016-02-19" NP980753.RAesDgX1L8z0wP8J-pMxO91P5bKn6i1reUA4xYn32X8Lo130_provenance.