Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_assertion description "[TET2 mutations improve the ELN molecular-risk classification in primary CN-AML because of their adverse prognostic impact in an otherwise favorable-risk patient subset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_assertion evidence source_evidence_literature NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_assertion SIO_000772 21343549 NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_assertion wasDerivedFrom befree-20150227 NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_assertion wasGeneratedBy ECO_0000203 NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914265.RACi_dfM3jkvoGXP4a0pN9bZrfSSub-tXglw5-DUPXpRg130_provenance.