Barely Significant
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Next-generation sequencing-based genetic landscape and its clinical implications for Chinese acute myeloid leukemia patients.

Cancer Cell Int · 2018 · PMC6303841 · PMID 30598640

1
hedged sentence
0.0560
closest p · 1.1× alpha
0.0560
boldest claim

The sentences

showed a trendp = 0.056so close (0.05 < p ≤ 0.1)
The older patient group also showed a trend of more DNMT3A (14.7% vs 5.4%, p = 0.056) and RUNX1 (11.8% vs 4.5%, p = 0.081) mutations than the younger patient group.

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