Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_assertion evidence source_evidence_literature NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_assertion SIO_000772 20398908 NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_assertion wasDerivedFrom gad-20130706 NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_assertion wasGeneratedBy ECO_0000203 NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP83665.RAX2ahGHKjY8mfmavkr-aMBDIcEz0KqXOGsQQNi2E34FA130_provenance.