Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_assertion description "[Recent studies are shedding light on the molecular basis of myelodysplasia and how mutations and epimutations can induce and promote this neoplastic process through aberrant transcription factor function (RUNX1, ETV6, TP53), kinase signalling (FLT3, NRAS, KIT, CBL) and epigenetic deregulation (TET2, IDH1/2, DNMT3A, EZH2, ASXL1, SF3B1, U2AF1, SRSF2, ZRSR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_assertion evidence source_evidence_literature NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_assertion SIO_000772 24903747 NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_assertion wasDerivedFrom befree-2016 NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_assertion wasGeneratedBy ECO_0000203 NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.
- befree-2016 importedOn "2016-02-19" NP1189374.RAVAcqB1RRQM_UFiCPDW5i7vKoIeTweMtqE_uaanBSYns130_provenance.