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- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_assertion type Assertion NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_head.
- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_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." NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_provenance.
- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_assertion evidence source_evidence_literature NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_provenance.
- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_assertion SIO_000772 11158219 NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_provenance.
- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_assertion wasDerivedFrom befree-20150227 NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_provenance.
- NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_assertion wasGeneratedBy ECO_0000203 NP859738.RAfVjRwBMUsennumsEU28KnTGvHzWpUBTg11B8vmcY2wA130_provenance.