Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion> ?p ?o ?g. }
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- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion type Assertion NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_head.
- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion description "[The K allele of the R219K variant was significantly more frequent in FH subjects without premature CHD (0.32, 95% CI 0.27 to 0.37) than in FH subjects with premature CHD (0.25, 95% CI 0.21 to 0.29) (p<0.05), suggesting that the genetic variant R219K in AB]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_provenance.
- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion evidence source_evidence_literature NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_provenance.
- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion SIO_000772 12624133 NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_provenance.
- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion wasDerivedFrom gad-20150221 NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_provenance.
- NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_assertion wasGeneratedBy ECO_0000203 NP61513.RAtPZqPLBZgyXN9HhdvaW3fsazxTsTJCTect-qzeA2uuc130_provenance.