Barely Significant
← all excerpts

Genetic variants in UNC93B1 predispose to childhood-onset systemic lupus erythematosus.

Nat Immunol · 2024 · PMC11147776 · PMID 38831104

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
Lupus-like disease in mice with the mutation UNC93B1 V117L Given that UNC93B1 V117L is a highly significant risk factor for childhood-onset SLE, but also present in the general population, we sought to confirm pathogenicity in vivo and created mice with the orthologous mutation V117L.

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.