Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_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." NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_assertion evidence source_evidence_literature NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_assertion SIO_000772 22537917 NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_assertion wasDerivedFrom befree-2016 NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_assertion wasGeneratedBy ECO_0000203 NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.
- befree-2016 importedOn "2016-02-19" NP977892.RAmeSXg4sdVy5bvw1sYGkp8nhF7qLqw2RLP0z9579PL4A130_provenance.