Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_assertion description "[Our results indicated that MET amplification was present in untreated NSCLC and EGFR mutation or MET amplification activated MET protein in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_assertion evidence source_evidence_literature NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_assertion SIO_000772 19117057 NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_assertion wasDerivedFrom befree-2016 NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_assertion wasGeneratedBy ECO_0000203 NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.
- befree-2016 importedOn "2016-02-19" NP711735.RAU0Aub5dJ36Dbz3Bwv316Ieb9l3ywYCqn3hGuCQ0F8Kc130_provenance.