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DESCRIBE <http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6>
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http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6
http://www.w3.org/2000/01/rdf-schema#comment
"Clinical exome sequencing identifies novel compound heterozygous mutations of the POMT2 gene in patients with limb-girdle muscular dystrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_D3F0BB831254393711AAA03579A4ECEB1CE9BFF7502C096031CA252FD7459D6B0144392C658F5D788E63B95F1480981D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6
http://purl.uniprot.org/uniprot/Q9UKY4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6
http://purl.uniprot.org/uniprot/#_Q9UKY4-mappedCitation-36217604
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/42161DD80BF447E79A50204A6C2199F82C1BEA276E3193CC0A7E8EB145616F3D6B41A4DEC8B85BA2047EEEC1DB6D5AD6