Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion description "[We examined 193 patients with myelodysplastic syndromes and 53 patients with acute myeloid leukemia arising from myelodysplastic syndromes for mutations in IDH1 (R132), IDH2 (R172 and R140), and NPM1 by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion evidence source_evidence_literature NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion SIO_000772 20494930 NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion wasDerivedFrom befree-20140225 NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion wasGeneratedBy ECO_0000203 NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance.