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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D>
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http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D
http://www.w3.org/2000/01/rdf-schema#comment
"Sanger sequencing of KRIT1 revealed 57 out of 80 (71.2%) identified points variants confirming that these mutations remain the most common genetic cause of cerebral cavernous malformation (CCM) in Italy."
xsd:string
http://purl.uniprot.org/uniprot/#_BB5F28A1573714EB2DF7AE5204D04A070CF3C901206A99B60B1BE89271CA4DF2A1728F954C4CD9A7453ABD745A303DC7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D
http://purl.uniprot.org/uniprot/A0A0C4DG23
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D
http://purl.uniprot.org/uniprot/#_A0A0C4DG23-mappedCitation-30161288
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E0D57D67B954E314CE5B390249AD47D69276CC057146C5339C5B4EBB268E8F192FE78E0C219B44906BEB7C8A2A6C871D