Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion> ?p ?o ?g. }
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- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion type Assertion NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_head.
- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_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." NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_provenance.
- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion evidence source_evidence_literature NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_provenance.
- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion SIO_000772 24903747 NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_provenance.
- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion wasDerivedFrom befree-20150227 NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_provenance.
- NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_assertion wasGeneratedBy ECO_0000203 NP286378.RAf_mpDMoaBV0D-Q6Waidv4ZRgGUh_lMWKGDjLj1HtFPY130_provenance.