Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_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." NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_assertion evidence source_evidence_literature NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_assertion SIO_000772 19388168 NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_assertion wasDerivedFrom befree-20140225 NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_assertion wasGeneratedBy ECO_0000203 NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381655.RA7kvCNhw3-Rq-eNc4S0OwU_nScuCCZTGQTzcZAqZ1uUI130_provenance.