Barely Significant
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Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA.

Sci Rep · 2022 · PMC9338264 · PMID 35906470

1
hedged sentence
0.0650
closest p · 1.3× alpha
0.0650
boldest claim

The sentences

showed a trendp = 0.065so close (0.05 < p ≤ 0.1)
Despite the small size of the ALL sub-cohort of relapsed patients with clinical data available (n = 13), the three patients with mutations showed a trend for shorter OS (HR, hazard ratio 6.4 95% CI 0.89–46.0.8, p = 0.065, Supplementary Fig.

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