Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_assertion description "[Hp2-1 was associated with a significant risk for celiac disease (P = 0.0006, odds ratio [OR] 1.54, 95% CI 1.20-1.98; prevalence 56.9% in patients vs 46.1% in controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_assertion evidence source_evidence_literature NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_assertion SIO_000772 18258668 NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_assertion wasDerivedFrom befree-20140225 NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_assertion wasGeneratedBy ECO_0000203 NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP427688.RAtQOpCSm_wzUgsnZfHJVAzUzgy1WVcLvKtbpGYvm5ZGA130_provenance.