Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_assertion description "[In total, 2,351 patients with MDS who have records in the German-Austrian and the MD Anderson Cancer Center databases were included and analyzed in univariate and multivariate models regarding overall survival and risk of transformation to acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_assertion evidence source_evidence_literature NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_assertion SIO_000772 21519021 NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_assertion wasDerivedFrom befree-2016 NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_assertion wasGeneratedBy ECO_0000203 NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP889521.RAmRFTV3hx1oVwd4TPWCwGMAAkUEPljE3q0WoajMEdKsQ130_provenance.