Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_assertion description "[We defined clinically relevant time points for NPM1(mut) MRD assessment that allow for the identification of patients with AML who are at high risk of relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_assertion evidence source_evidence_literature NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_assertion SIO_000772 21555683 NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_assertion wasDerivedFrom befree-2016 NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_assertion wasGeneratedBy ECO_0000203 NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP892738.RAmZNwPvIakp1BLjfTlzKWS2A8SsYoq9ew4eTNxaAKDEM130_provenance.