Barely Significant
← all excerpts

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis.

BMC Ophthalmol · 2021 · PMC7807486 · PMID 33446141

1
hedged sentence
closest p
boldest claim

The sentences

more or less significantno p-value reported
Afterwards, the slit-lamp examination revealed a more or less significant bilateral posterior subcapsular cataract.

also in 311 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.