Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_assertion description "[The present study evaluated single-nucleotide polymorphisms (SNPs) in XRCC3, XPD and Aurora kinase A in NSCLC patients in order to assess whether these biomarkers were able to predict the outcomes of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_assertion evidence source_evidence_literature NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_assertion SIO_000772 23053267 NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_assertion wasDerivedFrom befree-20140225 NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_assertion wasGeneratedBy ECO_0000203 NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP216652.RAtHtwzh3d0ssK7wMdU_7PZu_o2gpfjJthJaMGdw4Ceow130_provenance.