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DESCRIBE <http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036>
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http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036
http://www.w3.org/2000/01/rdf-schema#comment
"Wilson disease results from mutations of the ATP7B gene on chromosome 13."
xsd:string
http://purl.uniprot.org/uniprot/#_0B836C3A63E5B9D1B11E85B1F0FEAACCDCC0055D1FA1F7FDAEA3379C4F8223312763C15E62B7DE4DB7CF4E6FF4AC16C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036
http://purl.uniprot.org/uniprot/P35670
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036
http://purl.uniprot.org/uniprot/#_P35670-mappedCitation-16230279
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5602980CF5925317B5F628541944E9A7DD75DE9025083C88413E2664DD9F6562801B8EEE706C939F66962880803EA036