Barely Significant
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Premature Myocardial Infarction: Genetic Variations in SIRT1 Affect Disease Susceptibility.

Cardiol Res Pract · 2019 · PMC6501229 · PMID 31143479

Europe PMCDOI
1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

nearly significantp =0.06so close (0.05 < p ≤ 0.1)
The C allele was predominantly found in the patients group, nearly significant ( p =0.06) ( Table 5 ).

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