Barely Significant
← all excerpts

Impacts of genomic networks governed by human-specific regulatory sequences and genetic loci harboring fixed human-specific neuro-regulatory single nucleotide mutations on phenotypic traits of modern humans.

Chromosome Res · 2020 · PMC7480002 · PMID 32902713

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
1 ) and revealed a large scale of highly significant associations with a multitude of biological processes, molecular functions, genetic and metabolic pathways, cellular compartments, and gene expression perturbations (Supplemental Table Set S1 ).

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.