Barely Significant
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Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1.

PLoS Pathog · 2017 · PMC5690691 · PMID 29108000

Europe PMCDOI
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hedged sentence
0.0300
closest p · 0.6× alpha
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boldest claim

The sentences

nominally significantp = 0.03actually significant
The CD101 cytoplasmic PRV group was nominally significant (HR = 2.8, p = 0.03) ( Table 3 ; Fig 3A ), but not after Bonferroni adjustment for multiple testing (p = 0.09).

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