Barely Significant
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Pharmacogenetic associations of MMP9 and MMP12 variants with cardiovascular disease in patients with hypertension.

PLoS One · 2011 · PMC3160956 · PMID 21887284

Europe PMCDOI
2
hedged sentences
0.0400
closest p · 0.8× alpha
0.0480
boldest claim

The sentences

modestly significantP = 0.04actually significant
After adjusting for baseline characteristics, the association between the MMP9 R279Q variant and stroke was modestly significant, with participants carrying the minor G allele having decreased risk of stroke (HR = 1.00 for AA, 0.87 for GA, 0.91 for GG; P = 0.04, additive genetic model).

also in 257 other papers

marginally significantP = 0.048actually significant
The P -value for the pharmacogenetic effect was marginally significant ( P = 0.048).

also in 26,082 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.