Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_assertion description "[Mutations in the genes encoding the presenilins (PS1 and PS2) and amyloid precursor protein (APP) are associated with FAD, whereas mutations in the prion protein (PrP) gene are associated with prion disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_assertion evidence source_evidence_curated NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_assertion SIO_000772 10631141 NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_assertion wasDerivedFrom uniprot-20130724 NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_assertion wasGeneratedBy ECO_0000218 NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP441.RAuNKEUI7knVbyeaaXrglbP5_qSaR6AiCg30DyMPA1KPo130_provenance.