Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_assertion description "[Ninety-six somatic mutations in key oncogenic drivers of mCRC and 133 common single-nucleotide polymorphisms (SNPs) in vascular endothelial growth factor (VEGF) pathway genes were analysed, and 27 plasma markers measured at baseline, during and after treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_assertion evidence source_evidence_literature NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_assertion SIO_000772 26355232 NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_assertion wasDerivedFrom befree-2016 NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_assertion wasGeneratedBy ECO_0000203 NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293927.RA-SUil9z342lVRjyAAfM3Du9cU8hS2tDX9l5ryK2O_W8130_provenance.