Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_assertion description "[Furthermore, the frequencies of STC-1 mRNA expression detected in PB and BM were 37.6% (32/85) and 21.2% (18/85), respectively, and together increased sensitivity to 48.2% (41/85), which was much higher than that in patients with benign esophageal disease (5.0%, 2/40, P < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_assertion evidence source_evidence_literature NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_assertion SIO_000772 22537917 NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_assertion wasDerivedFrom befree-20150227 NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_assertion wasGeneratedBy ECO_0000203 NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP718335.RAHUdjtHDl4g5clqB-nX2xZo0f2W-7GgL5iMgNjhDi0D0130_provenance.