Barely Significant
← all excerpts

An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.

Mol Vis · 2012 · PMC3324362 · PMID 22509102

Europe PMC
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp=0.0001298actually significant
The heritability of SPH or SEM was highly significant (p=0.0001298 and p=0.0000006 for SPH and SE, respectively), with heritabilities of 23.2% (SPH) and 33.9% (SE).

also in 132,142 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.