Barely Significant
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Decoding ancestry-specific genetic risk: interpretable deep feature selection reveals prostate cancer SNP disparities in diverse populations.

BioData Min · 2025 · PMC12481780 · PMID 41024066

Europe PMCDOI
1
hedged sentence
0.0000
closest p · 0.0× alpha
0.0000
boldest claim

The sentences

highly significantp = 5.9 × e-7actually significant
The combined allelic test was highly significant, with p = 5.9 × e-7.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.