Barely Significant
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Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

PLoS One · 2016 · PMC4892567 · PMID 27257688

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a clear trendno p-value reported
A clear trend of increased percentage of cases with increasing risk score is observed.

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an increasing trendno p-value reported
An increasing trend of OR values with increasing number of risk alleles is apparent from the plot ( Fig 3 ).

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highly significantno p-value reported
Given these highly significant results, the observed AUC probably indicates that this study has substantial power to confer these genetic variants as predictors of risk 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.