Barely Significant
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Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe.

Allergy Asthma Clin Immunol · 2013 · PMC3751114 · PMID 23937903

Europe PMCDOI
2
hedged sentences
0.0510
closest p · 1.0× alpha
0.0510
boldest claim

The sentences

almost significantp = 0.051so close (0.05 < p ≤ 0.1)
The difference observed in the delay in diagnosis between patients with HAE type I and patients with HAE type II was almost significant (8.0 [0.0–62.0] versus 21.0 years [0.0–42.0]; p = 0.051).

also in 1,858 other papers

did not quite reach statistical significanceno p-value reported
The median delay in diagnosis was longer for HAE type II versus type I (21 versus 8 years, respectively), although this did not quite reach statistical significance.

also in 679 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.