Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion> ?p ?o ?g. }
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- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion type Assertion NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_head.
- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_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." NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_provenance.
- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion evidence source_evidence_literature NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_provenance.
- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion SIO_000772 17914026 NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_provenance.
- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion wasDerivedFrom lhgdn-20090331 NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_provenance.
- NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_assertion wasGeneratedBy ECO_0000203 NP178856.RAnzvGBrA8VjraJLqDslWG4NFHffjTsW2QS0_RqtSA4Sc130_provenance.