Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion> ?p ?o ?g. }
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- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion type Assertion NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_head.
- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_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." NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_provenance.
- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion evidence source_evidence_literature NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_provenance.
- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion SIO_000772 15009458 NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_provenance.
- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion wasDerivedFrom befree-20150227 NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_provenance.
- NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_assertion wasGeneratedBy ECO_0000203 NP877023.RAEKcEfOpDLUXxkdjB_v4oh5Y0-8sQREmdX2eHXpbpPVE130_provenance.