Barely Significant
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Frequency and variability of genomic rearrangements on MSH2 in Spanish Lynch Syndrome families.

PLoS One · 2013 · PMC3770653 · PMID 24039744

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According to our data, the 55% of LGR carriers developed CRC compare with 42% in punctual mutation carries however this difference did not reach statistical significance.

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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.