Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP734261.RAFhiI1injbM4zVbKvoSXxszoj9pMe2pKJYnXHjmP2a6Q130_provenance.