Barely Significant
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HRAS mutation prevalence and associated expression patterns in pheochromocytoma.

Genes Chromosomes Cancer · 2016 · PMC4794776 · PMID 26773571

1
hedged sentence
0.0800
closest p · 1.6× alpha
0.0800
boldest claim

The sentences

did not reach statistical significanceP = 0.08so close (0.05 < p ≤ 0.1)
Regarding clinical parameters, no mutations were found in PPGLs classified as malignant according to the current WHO criteria and the patients endowed with a HRAS mutation tended to have higher age at diagnosis (mean 63 ±10 years) compared with those without HRAS mutation (mean 54 ±16 years) however this association did not reach statistical significance (two‐tailed Mann–Whitney U ‐test, P = 0.08).

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