Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_assertion description "[The results showed the frequency of the Asp299Gly genotype was increased in patients with chronic disease (OR 25.3, 95% CI 5.2-115.6, P�<�0.001) and patients with acute disease (OR 8.03, 95% CI 1.7-37.7, P�=�0.006) compared to LST negative subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_assertion evidence source_evidence_literature NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_assertion SIO_000772 21056683 NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_assertion wasDerivedFrom befree-20140225 NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_assertion wasGeneratedBy ECO_0000203 NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.
- befree-20140225 importedOn "2014-02-25" NP827028.RA4I4yC4hNZTSgP0Qq1xRhg499qPc4LE45wWvd92HWI54130_provenance.