Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion wasGeneratedBy ECO_0000203 NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion wasDerivedFrom befree-20150227 NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion SIO_000772 20466522 NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion evidence source_evidence_literature NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.
- NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_assertion description "[Other variants, identified in controls, included c.2089G>A (p.Gly697Ser) and c.2097T>C. Our identification of potentially defective NPAS3 variants supports recent studies that implicate perturbations in NPAS3 pathways in impaired neurogenesis and psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936868.RAYQMWEAr1U4ZwW8ouVvO480VfV_00Xkhcp2FY9DrE0-s130_provenance.