Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion> ?p ?o ?g. }
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- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion type Assertion NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_head.
- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion wasGeneratedBy ECO_0000203 NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_provenance.
- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion wasDerivedFrom befree-2016 NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_provenance.
- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion SIO_000772 20531469 NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_provenance.
- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion evidence source_evidence_literature NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_provenance.
- NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_assertion description "[When comparing 996 ASD individuals of European ancestry to 1,287 matched controls, cases were found to carry a higher global burden of rare, genic copy number variants (CNVs) (1.19 fold, P = 0.012), especially so for loci previously implicated in either ASD and/or intellectual disability (1.69 fold, P = 3.4 x 10(-4)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817329.RAUkmi6W8jlfwAodEVLuQDqKLfaueJF24ABaeFI52KToU130_provenance.