Barely Significant
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Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.

PLoS One · 2010 · PMC2966418 · PMID 21060786

Europe PMCDOI
1
hedged sentence
0.0036
closest p · 0.1× alpha
0.0036
boldest claim

The sentences

highly significantp = 0.0036actually significant
The difference between ICCA patients and control individuals was statistically highly significant (p = 0.0036 for ICCA.SRa and p = 0.0001 for ICCA.SRb, Mann-Whitney test; p = 0.0049 for ICCA.SRa and p = 0.0001 for ICCA.SRb, unpaired t-test with Welch's correction).

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