Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_assertion description "[In individuals with autism spectrum disorders (ASDs), several studies have found SHANK3 to be disrupted by deletions ranging from hundreds of kilobases to megabases, suggesting that 1% of individuals with ASDs may have these chromosomal aberrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_assertion evidence source_evidence_literature NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_assertion SIO_000772 19384346 NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_assertion wasDerivedFrom befree-2016 NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_assertion wasGeneratedBy ECO_0000203 NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.
- befree-2016 importedOn "2016-02-19" NP733979.RACeUaDqBDLz8Z6Zsdo_wc-0TK6tSjSzJYlkHQSeIQIrg130_provenance.