Barely Significant
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Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

Genome Med · 2017 · PMC5693798 · PMID 29149916

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nominally significantno p-value reported
Both NEK1 and SOD1 were nominally significant in our Chinese sample, while TBK1 was not significant (Table 1 ), and the case-control frequencies of rare coding variants were similar to Europeans ( NEK1 1.8%/0.4% vs 1.9%/0.8%; SOD1 : 1.5%/0.2% vs 0.9%/0.1%; TBK1 : 1.2%/0.2% vs 1.4%/0.4%).

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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.