Matches in Nanopublications for { ?s ?p "[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 ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_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 ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP929647.RAJKGwcHNxADydO4FoUh48zmoICjWhuD35iqM13O2AVkM130_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 ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929647.RAJKGwcHNxADydO4FoUh48zmoICjWhuD35iqM13O2AVkM130_provenance.