Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion> ?p ?o ?g. }
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- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion type Assertion NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_head.
- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion description "[The aim of the present study was to clarify whether factor H mutations were involved in genetic predisposition to hemolytic uremic syndrome, by performing linkage and mutation studies in a large number of patients from those referred to the Italian Registry for Recurrent and Familial HUS/TTP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_provenance.
- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion evidence source_evidence_literature NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_provenance.
- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion SIO_000772 11158219 NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_provenance.
- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion wasDerivedFrom befree-20140225 NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_provenance.
- NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_assertion wasGeneratedBy ECO_0000203 NP832585.RAFLCNAfEiq7PI6GnLkf4M5pWF6hFbyp2XGor9Jx94Les130_provenance.