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DESCRIBE <http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD>
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http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD
http://www.w3.org/2000/01/rdf-schema#comment
"Deficiency of liver glycogen phosphorylase is predominantly the result of missense mutations affecting enzyme activity. There are no common mutations and the severity of clinical symptoms varies significantly."
xsd:string
http://purl.uniprot.org/uniprot/#_B19D5DD2546E1D05B45C774FADA7715B51117336209F5341769894ADE436BAB228BD9E8508F54C4CFA6E726592B30FEF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD
http://purl.uniprot.org/uniprot/P06737
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD
http://purl.uniprot.org/uniprot/#_P06737-mappedCitation-17705025
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0EB5DCFD5C0662FD60CCD42F5B221DD4190040421260BFB658ABA36D84EAD84AEB6FF5704E52C6A6E6AEDC5C91AD52BD