Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_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." NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_assertion evidence source_evidence_literature NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_assertion SIO_000772 21782286 NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_assertion wasDerivedFrom befree-20140225 NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_assertion wasGeneratedBy ECO_0000203 NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP515997.RAX_PVBGI-7SnLqeejOtsS4JFYE6H9Oijb2DrR89S4Mho130_provenance.