Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_assertion description "[Through a case-control study and a reporter assay, we investigated the association of PPP2R2B CAG repeat polymorphism with Taiwanese AD, essential tremor (ET), Parkinson's disease (PD), and schizophrenia and clarified the functional implication of this polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_assertion evidence source_evidence_literature NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_assertion SIO_000772 18484086 NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_assertion wasDerivedFrom befree-20150227 NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_assertion wasGeneratedBy ECO_0000203 NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP638809.RAdAf7hxd1M0wSemeEBrqqWtjLiuS19EEvs0DGCQGSh5k130_provenance.