Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion> ?p ?o ?g. }
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- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion type Assertion NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_head.
- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_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." NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion evidence source_evidence_literature NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion SIO_000772 19388168 NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion wasDerivedFrom befree-2016 NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_assertion wasGeneratedBy ECO_0000203 NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.