Barely Significant
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Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

PLoS One · 2012 · PMC3531408 · PMID 23300620

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nominally significantno p-value reported
Even if some nominally significant associations were found with the first cohort, their number, nature and strength did not argue for their usefulness in clinical practice.

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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.