Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_assertion description "[These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_assertion evidence source_evidence_literature NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_assertion SIO_000772 21782286 NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_assertion wasDerivedFrom befree-20140225 NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_assertion wasGeneratedBy ECO_0000203 NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817587.RAcr46AV-lCWADqdagPaWyPFvxyUIOG0JerR14kOnQf6U130_provenance.