Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion> ?p ?o ?g. }
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- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion type Assertion NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_head.
- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion description "[ADAMTS13 severe enzymatic deficiency and mutations have been described in the congenital thrombotic thrombocytopenic purpura (TTP or Upshaw-Schulman syndrome), a rare and severe disease related to multivisceral microvascular thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion evidence source_evidence_literature NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion SIO_000772 15009458 NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion wasDerivedFrom befree-2016 NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_assertion wasGeneratedBy ECO_0000203 NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.