Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP434827.RAgInhHe3d0ra1maZw5uyGfNhrQPyoK48ExzNhxh5xAWY130_provenance.