Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_assertion wasGeneratedBy ECO_0000218 NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_assertion wasDerivedFrom uniprot-20130724 NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_assertion SIO_000772 11755616 NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_assertion evidence source_evidence_curated NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_assertion description "[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy) is a small-artery disease of the brain caused by NOTCH3 mutations that lead to an abnormal accumulation of NOTCH3 within the vasculature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4547.RA5R362mNATh2R2tvXtqI4t_ZW7JJgoSM3HEEEV0wfn_c130_provenance.