Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_assertion description "[Here we demonstrate that runx1 deletion in mice induces the persistence of MYH10 in platelets, and a similar persistence was observed in platelets of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (chronic myelomonocytic leukemia) RUNX1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_assertion evidence source_evidence_literature NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_assertion SIO_000772 22677128 NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_assertion wasDerivedFrom befree-20150227 NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_assertion wasGeneratedBy ECO_0000203 NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583699.RAXTpe0LsjV0_ynXgVbtGH3gls0CWHQdb0WmETBv-J2XQ130_provenance.