Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_assertion description "[Multivariate analysis revealed that mutant FBXW7 was an independent prognostic indicator for inferior EFS (hazard ratio [HR] 4.38; 95�% confidence interval [CI] 1.15-16.71; p?=?0.03) and tended to be associated with reduced OS (HR 2.81; 95�% CI 0.91-8.69; p?=?0.074) in pediatric T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_assertion evidence source_evidence_literature NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_assertion SIO_000772 26341754 NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_assertion wasDerivedFrom befree-2016 NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_assertion wasGeneratedBy ECO_0000203 NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293737.RAsUM-TtEs2HHUSWV2lpkpJqrGUzzUaWc62yGf9sJXMWc130_provenance.