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DESCRIBE <http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3>
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http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3
http://www.w3.org/2000/01/rdf-schema#comment
"association between the c.2299insC mutation and hepatic phenotype and between the p. Ala1003Thr mutation and neurologic phenotype in Wilson disease in a large Lebanese family"
xsd:string
http://purl.uniprot.org/uniprot/#_A1C43CACD9A6A55E5E9E0ED9112F89C441EC530ABC1DAA3FCE92A80186B14E66A68741CA606CD52954845D72E04D644B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3
http://purl.uniprot.org/uniprot/C8BMD5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3
http://purl.uniprot.org/uniprot/#_C8BMD5-mappedCitation-25390358
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5923CBE9DEA0B083884E14140705C69013F69110A219826399A697A3DFF79BCD679809D7FB2B85011737BB9D05989AC3