Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_assertion wasGeneratedBy ECO_0000203 NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_assertion wasDerivedFrom befree-20140225 NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_assertion SIO_000772 14872021 NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_assertion evidence source_evidence_literature NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_assertion description "[Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817562.RAB4UyFcxqHGYvE8kCGLdpkYQxiDbxCS-Dvg1iiZ4M_aU130_provenance.