Barely Significant
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Recurrent mutations, including NPM1c, activate a BRD4-dependent core transcriptional program in acute myeloid leukemia.

Leukemia · 2014 · PMC3918873 · PMID 24220271

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hedged sentence
0.0080
closest p · 0.2× alpha
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boldest claim

The sentences

highly significantP =0.008actually significant
Of specific relevance for human AML, in leukemia driven by both NPM1c and a FLT3 activating mutation a highly significant survival advantage was demonstrated ( P =0.008)( Figure 6d ).

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