Barely Significant
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NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study.

Oncotarget · 2016 · PMC5085110 · PMID 27191271

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highly significantno p-value reported
These results suggest rs700926 in NPR-C located in Chr 5p confers a highly significant risk of CAD in the northern and southern Chinese Han populations and that rs700926 may represent a new susceptibility locus for CAD.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.