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DESCRIBE <http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2>
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http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2
http://www.w3.org/2000/01/rdf-schema#comment
"a distinct SCA (spinocerebellar ataxia)phenotype (SCA27) is associated with a F145S mutation in the fibroblast growth factor 14 (FGF14) gene on chromosome 13q34."
xsd:string
http://purl.uniprot.org/uniprot/#_7071BA297A6F6ABED042971CF5E830230ED97A17B83C3D3A7FFE82D0C981A64B70CA7CCB4C2BDD688F81B8427FC90F66
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2
http://purl.uniprot.org/uniprot/Q92915
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2
http://purl.uniprot.org/uniprot/#_Q92915-mappedCitation-16211615
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A4EE898F69831E698A7C2ED587E0012A5464929B9FC25011356D20404B8CDA77F5688E1A51B7B030B63D9C92E9F4EBA2