Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_assertion wasGeneratedBy ECO_0000203 NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_assertion wasDerivedFrom befree-20150227 NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_assertion SIO_000772 24075799 NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_assertion evidence source_evidence_literature NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.
- NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_assertion description "[Our findings do not support the hypothesis that the common VDR gene variants investigated in this study are of clinical relevance with respect to CRC prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346347.RAN0bqT4lw5FMBFzJPoIvMTUUsgu3EI--t9wnURZODCa0130_provenance.