Barely Significant
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Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis.

BMC Med Genomics · 2021 · PMC7780652 · PMID 33397358

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The sentences

highly significantno p-value reported
Highly significant association of this region was observed with either the disease or its endophenotypes in many populations [ 8 , 15 – 22 ] specifically with IOP.

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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.