Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_assertion description "[Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_assertion evidence source_evidence_literature NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_assertion SIO_000772 17914026 NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_assertion wasDerivedFrom befree-20140225 NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_assertion wasGeneratedBy ECO_0000203 NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828807.RAOQRIK3nvDcsmgn1l3xhmTASBskDbGF4Fp-sCCfQwIMQ130_provenance.