Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_assertion wasGeneratedBy ECO_0000203 NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_assertion wasDerivedFrom befree-2016 NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_assertion SIO_000772 9627113 NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_assertion evidence source_evidence_literature NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.
- NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_assertion description "[Investigation of mutations in exon 8, especially codon 273 mutation and mutant H2 alpha helix was considered to be a clinically useful approach for determining the prognosis of patients with NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397401.RAIv9uK-BncNAsZtFsfCeSuFx2CwSqaThiegM-hWK9lVw130_provenance.