Barely Significant
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DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects.

Sci Rep · 2015 · PMC4486972 · PMID 26130459

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highly significantno p-value reported
Measured differences were highly significant with a p-value of 1.205 × 10 −6 [Mann-Whitney-U test].

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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.