Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_assertion description "[The functional effects of risk variants at the level of cognition and connectivity has been described and recently, ZNF804A has been identified, and the MHC re-identified as risk loci, and it has been shown that at least a third of the variation in liability is due to multiple common risk variants of small effect with a substantial shared genetic liability between schizophrenia and bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_assertion evidence source_evidence_literature NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_assertion SIO_000772 19818200 NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_assertion wasDerivedFrom befree-2016 NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_assertion wasGeneratedBy ECO_0000203 NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.
- befree-2016 importedOn "2016-02-19" NP768584.RA2I_QgvNAJGyw2gJ1D1E4yxa2ZAO7HLOOGw_xfd04Q9c130_provenance.