Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion> ?p ?o ?g. }
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- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion type Assertion NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_head.
- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_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." NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_provenance.
- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion evidence source_evidence_literature NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_provenance.
- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion SIO_000772 19388168 NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_provenance.
- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion wasDerivedFrom befree-20140225 NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_provenance.
- NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_assertion wasGeneratedBy ECO_0000203 NP376451.RAokM2ppRkyoGmfLzwQx1zwDpEmds_lKOjg2FB9G4eCOk130_provenance.