Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_assertion description "[Mutations in the CFH gene are associated with atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis type II and C3 glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_assertion evidence source_evidence_literature NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_assertion SIO_000772 21270828 NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_assertion wasDerivedFrom befree-20140225 NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_assertion wasGeneratedBy ECO_0000203 NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189932.RAo8kCn2dWOlfdMfqWjnLgWBizR0AIE3bOFgUBG4V9T5A130_provenance.