Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.

J Am Heart Assoc · 2015 · PMC4599414 · PMID 25964206

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

highly significantno p-value reported

Although the association of p.R4810K was reported to be highly significant and reproducible, the disease susceptibility of other RNF213 variants remains largely unknown.

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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.