Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion> ?p ?o ?g. }
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- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion type Assertion NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_head.
- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion wasGeneratedBy ECO_0000203 NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_provenance.
- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion wasDerivedFrom befree-2016 NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_provenance.
- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion SIO_000772 24807205 NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_provenance.
- NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_assertion evidence source_evidence_literature NP1180433.RAUCJl1kPoInzrXM-TTVhs9L58qPil1-HP55yRag94bG0130_provenance.
- 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.