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DESCRIBE <http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F>
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http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F
http://www.w3.org/2000/01/rdf-schema#comment
"A human-specific deletion in mouse Cmah increases disease severity in the mdx model of Duchenne muscular dystrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_05EF0CB12DE618667188A29B8AE10F472B08CF2C16B922A89A5EF604E49638A23763B14FF69918BD68B5B3E33F5E9FFD
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F
http://purl.uniprot.org/uniprot/Q61419
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F
http://purl.uniprot.org/uniprot/#_Q61419-mappedCitation-20668298
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B4B4573DCC1792903FA65806115F888583DA1D9B72E151701D1973E52747E864F97A02DEACAF26241FB8E3293ECA51F