Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_assertion description "[Mutations in the Factor H gene are associated with severe and diverse diseases including the rare renal disorders hemolytic uremic syndrome (HUS) and membranoproliferative glomerulonephritis (MPGN) also termed dense deposit disease (DDD), as well as the more frequent retinal disease age related macular degeneration (AMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_assertion evidence source_evidence_literature NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_assertion SIO_000772 19388168 NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_assertion wasDerivedFrom befree-2016 NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_assertion wasGeneratedBy ECO_0000203 NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.
- befree-2016 importedOn "2016-02-19" NP734264.RAvfu-WZZ2fgFNR7eQhUhRK7NTK8PSb3m5JRD1lmkhKkE130_provenance.