Barely Significant
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Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I

eNeuro · 2015 · PMC4596087 · PMID 26464974

1
hedged sentence
0.0520
closest p · 1.0× alpha
0.0520
boldest claim

The sentences

not quite significantp = 0.052so close (0.05 < p ≤ 0.1)
The effect of genotype was not quite significant ( p = 0.052, F (1,15) = 4.42).

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