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DESCRIBE <http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D>
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http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D
http://www.w3.org/2000/01/rdf-schema#comment
"Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I."
xsd:string
http://purl.uniprot.org/uniprot/#_6881E84A3D750C5A234ED3C1CF4D2A72FCF17C415B027E6E6D5A445AF468EB8CBFB63AACB5C616A9B0658A34A42E9DDB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D
http://purl.uniprot.org/uniprot/B2RCY4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D
http://purl.uniprot.org/uniprot/#_B2RCY4-mappedCitation-20133649
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EB75F1BF598A33EE858EB6696C50FEB4375393D43935F8EBEBFB3395BCC4C1D04E642832223AB352D8E66C4B3FE7234D