Barely Significant
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Predisposition to cancer caused by genetic and functional defects of mammalian Atad5.

PLoS Genet · 2011 · PMC3161924 · PMID 21901109

1
hedged sentence
0.4800
closest p · 9.6× alpha
0.4800
boldest claim

The sentences

did not reach statistical significanceP = 0.48not close (p > 0.1)
The frequency of somatic ATAD5 mutations was higher among NEECs (6.0%, 4 of 66) than EECs (2.3%, 1 of 42), although this difference did not reach statistical significance ( P = 0.48, Fisher's exact test of significance).

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