Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion> ?p ?o ?g. }
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- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion type Assertion NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_head.
- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion description "[Functional deficiency or absence of the human von Willebrand factor (VWF)-cleaving protease (VWF-cp), recently termed ADAMTS13, has been shown to cause acquired and congenital thrombotic thrombocytopenic purpura (TTP), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_provenance.
- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion evidence source_evidence_literature NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_provenance.
- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion SIO_000772 15869605 NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_provenance.
- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion wasDerivedFrom befree-2016 NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_provenance.
- NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_assertion wasGeneratedBy ECO_0000203 NP492961.RADYZ-LJ5tn7INPlxddIL2DPcaKw-pWaVECF32MQRsGdA130_provenance.