RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/SHA-384/341C697814C85CAB8651CE5573098F91074914A5B751969038206193B485F6B6FDB927132AC43826B3DD9E0B7481C206http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/341C697814C85CAB8651CE5573098F91074914A5B751969038206193B485F6B6FDB927132AC43826B3DD9E0B7481C206http://www.w3.org/2000/01/rdf-schema#comment"These studies provide the first evidence in patients with a RUNX1 mutation for a defect in AH (lysosomal) secretion and for a global defect in secretion involving all three types of platelet granules that is unrelated to a granule content deficiency. They highlight the pleiotropic effects and multiple platelet defects associated with RUNX1 mutations."xsd:string
http://purl.uniprot.org/uniprot/#_F015797DA7D412B5A65820578DAA3D729916F850BD33622F244D312E92BACFDDBA18BC96856A1818AE82BBBF26C9215Ahttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/341C697814C85CAB8651CE5573098F91074914A5B751969038206193B485F6B6FDB927132AC43826B3DD9E0B7481C206
http://purl.uniprot.org/uniprot/A0A0C4DG58http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/341C697814C85CAB8651CE5573098F91074914A5B751969038206193B485F6B6FDB927132AC43826B3DD9E0B7481C206
http://purl.uniprot.org/uniprot/#_A0A0C4DG58-mappedCitation-28662545http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/341C697814C85CAB8651CE5573098F91074914A5B751969038206193B485F6B6FDB927132AC43826B3DD9E0B7481C206