Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_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." NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_assertion evidence source_evidence_literature NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_assertion SIO_000772 24903747 NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_assertion wasDerivedFrom befree-20150227 NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_assertion wasGeneratedBy ECO_0000203 NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP286358.RAM9TXWMf-lJGGAU7g2enFHXlkGRBS1SxWkoBYZeZy0lk130_provenance.