Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_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." NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_assertion evidence source_evidence_literature NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_assertion SIO_000772 19384346 NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_assertion wasDerivedFrom befree-20140225 NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_assertion wasGeneratedBy ECO_0000203 NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP578931.RAJ9Djp7enyuIg_ATh3GxCwGAvNDug48fdNKSvvvNIrmk130_provenance.