Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_assertion description "[Both GST IIe/val and GST val/val genotypes were significantly more frequent in the patients with cirrhosis than in the normal carriers (p=0.001, OR: 12.160 95% CI 1.618-91.360 and p<0.001, OR: 32.154, 95% CI 4.585-225.513 respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_assertion evidence source_evidence_literature NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_assertion SIO_000772 19102379 NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_assertion wasDerivedFrom befree-2016 NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_assertion wasGeneratedBy ECO_0000203 NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.
- befree-2016 importedOn "2016-02-19" NP710722.RAC-4ddVG-fYNAuSiztt3zvvWEGNvJk_f3BYJLFID2DhM130_provenance.