The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia · 2017 · PMC5628133 · PMID 28321123

Europe PMC DOI

hedged sentence

0.1800

closest p · 3.6× alpha

0.1800

boldest claim

The sentences

did not reach statistical significanceP =0.18not close (p > 0.1)

Although those mutations were also more frequent in our t(8;21) cohort (13 vs 6% in patients with inv(16)), the difference did not reach statistical significance ( P =0.18).

also in 111,027 other papers

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.