Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_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." NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_assertion evidence source_evidence_literature NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_assertion SIO_000772 19384346 NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_assertion wasDerivedFrom gad-20130706 NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_assertion wasGeneratedBy ECO_0000203 NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP79341.RAwXz1258b5d1SZ40SwWdlCiYhK0lxPoalUNMCyYSqJEw130_provenance.