Barely Significant
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Prevalence of variations in melanoma susceptibility genes among Slovenian melanoma families.

BMC Med Genet · 2008 · PMC2556318 · PMID 18803811

1
hedged sentence
0.2570
closest p · 5.1× alpha
0.2570
boldest claim

The sentences

did not reach statistical significancep = 0.257not close (p > 0.1)
The p16INK4A mutation-carriers in our study developed CM earlier than the patients without mutation, but the difference did not reach statistical significance (p = 0.257).

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