Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_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." NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_assertion evidence source_evidence_literature NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_assertion SIO_000772 24903747 NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_assertion wasDerivedFrom befree-20150227 NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_assertion wasGeneratedBy ECO_0000203 NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP286349.RAKsXTkujSQUxFk5zA_IHqWW3cJvPjRjiMwnIM1sDsnwU130_provenance.