Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_assertion description "[The variant HNMT allele frequencies were slightly higher among patients with asthma [16.0%, 95% confidence interval (CI) 12.0-20.0] and among patients with rhinitis (13.2, 95% CI 10.3-16.1) as compared with healthy subjects (11.5 95% CI 8.9-14.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_assertion evidence source_evidence_literature NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_assertion SIO_000772 17651147 NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_assertion wasDerivedFrom befree-2016 NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_assertion wasGeneratedBy ECO_0000203 NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.
- befree-2016 importedOn "2016-02-19" NP621462.RAEyjomomSOfzP5MntfttycweyDen3xniwv8b8sZa9Q7w130_provenance.