Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_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." NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_assertion evidence source_evidence_literature NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_assertion SIO_000772 19818200 NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_assertion wasDerivedFrom befree-2016 NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_assertion wasGeneratedBy ECO_0000203 NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.
- befree-2016 importedOn "2016-02-19" NP768589.RA5WA1B78B0chI39hSMw5FSlfoL3hVT0pWXh1C-XPm5QA130_provenance.