Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_assertion description "[The poor prognosis of patients with single PIK3CA mutation in NSCLC and the prognostic value of PIK3CA mutation in EGFR/KRAS wildtype subgroup suggest the distinct mutation status of PIK3CA gene should be determined for individual therapeutic strategies in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_assertion evidence source_evidence_literature NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_assertion SIO_000772 24533074 NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_assertion wasDerivedFrom befree-2016 NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_assertion wasGeneratedBy ECO_0000203 NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1155812.RAzV9ILbJ4hXG_FnvUmxgsZMiP3g2zJUYcPB7fmxjZMJA130_provenance.