Barely Significant
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An Analysis of the Filaggrin Gene Polymorphism in Korean Atopic Dermatitis Patients.

J Korean Med Sci · 2016 · PMC4901008 · PMID 27366014

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highly significantno p-value reported
Highly significant association of the FLG null mutations with eczema and concomitant asthma have been replicated.

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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.