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DESCRIBE <http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E>
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http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E
http://www.w3.org/2000/01/rdf-schema#comment
"A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum."
xsd:string
http://purl.uniprot.org/uniprot/#_736FDA975C8909CCBAE2AF5F4581F89C777A281FA40D9D2DC3454E03CB6B561A837105B67DD8FFEEF0CB3A2AEE3DB10B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E
http://purl.uniprot.org/uniprot/Q9BV10
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E
http://purl.uniprot.org/uniprot/#_Q9BV10-mappedCitation-34467644
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9F818DF0D81B101776A6CB0F79A0FE43D1850CA24987AA57D2A78328F10DD56F8ED0555A51CB2C9F4CF5C6A627A3116E