Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_assertion wasGeneratedBy ECO_0000203 NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_assertion wasDerivedFrom befree-20150227 NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_assertion SIO_000772 23293110 NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_assertion evidence source_evidence_literature NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.
- NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_assertion description "[Combined analysis for DFS and OS indicated that patients with the fewest number of favorable genotypes simultaneously present (VEGFR-2 -906 T/T, CXCR-2 +1208 C/T or C/C and PAR-1 -506 Del/Del) were at the highest risk for recurrence or death (P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502844.RAtEBUR9FU--uMsJlGfIsEjlB34GP7aburJBzsDrKeAJY130_provenance.