Barely Significant
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KRAS mutation is a weak, but valid predictor for poor prognosis and treatment outcomes in NSCLC: A meta-analysis of 41 studies.

Oncotarget · 2016 · PMC4884999 · PMID 26840022

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borderline significantno p-value reported
Thus borderline significant associations of KRAS mutation with inferior treatment outcomes were observed.

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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.