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DESCRIBE <http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776>
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http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776
http://www.w3.org/2000/01/rdf-schema#comment
"Sequence alterations were identified in ATP7B some identified as intragenic deletions in Chinese Wilson's disease patients."
xsd:string
http://purl.uniprot.org/uniprot/#_CE94DE2C2A86F0CADD48827F6FFC45085F207056D74A1806BE8AA8324257BB14A7316EBB9AEC0432206EC8150D5BE28D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776
http://purl.uniprot.org/uniprot/P35670
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776
http://purl.uniprot.org/uniprot/#_P35670-mappedCitation-30655162
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CB7C87EAAAEE1A1E96B98389564FF1DFB51B8444A15B794ADD822181742E41BAA796C3FD825EAAEB5146B4C72B4D6776