Matches in Nanopublications for { ?s ?p "[We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have previously been associated with developmental verbal dyspraxia, and from variants in the CNTNAP2 gene, which have been associated with specific language impairment (SLI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion description "[We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have previously been associated with developmental verbal dyspraxia, and from variants in the CNTNAP2 gene, which have been associated with specific language impairment (SLI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_provenance.
- assertion description "[We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have previously been associated with developmental verbal dyspraxia, and from variants in the CNTNAP2 gene, which have been associated with specific language impairment (SLI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.