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DESCRIBE <http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718>
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http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718
http://www.w3.org/2000/01/rdf-schema#comment
"Our data suggest that screening for large RASA1 deletions and duplications in this disorder is important and suggest that NGS multi-gene panel testing is beneficial for the molecular diagnosis of cases with complex vascular phenotypes."
xsd:string
http://purl.uniprot.org/uniprot/#_3F56497440BEF849CA2B23DE30A66A681FE6F182A9B64B3AD2D84F89B3AC870C719A967A65F001C65AFD58E25D00E999
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718
http://purl.uniprot.org/uniprot/Q7Z4M2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718
http://purl.uniprot.org/uniprot/#_Q7Z4M2-mappedCitation-29891884
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/973FB0C28E6CC69F97B00789DE568EA2F3FB6941D476E1C5E4C8EB9B876771D9E98288F239E745C46E56C1B999CDC718