Barely Significant
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A genomic pathway approach to a complex disease: axon guidance and Parkinson disease.

PLoS Genet · 2007 · PMC1904362 · PMID 17571925

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highly significantno p-value reported
All three models in the secondary dataset were also highly significant.

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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.