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DESCRIBE <http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D>
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http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D
http://www.w3.org/2000/01/rdf-schema#comment
"OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium."
xsd:string
http://purl.uniprot.org/uniprot/#_7D0BC23B119E56F18C722D8D9B1D345A0AE27EBBDB7496D19E798ABDAA2D850BA7904CEC3F621E3666D1B16EE3927BC0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D
http://purl.uniprot.org/uniprot/F1T0D0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D
http://purl.uniprot.org/uniprot/#_F1T0D0-mappedCitation-25293953
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8DAA07BD3CB4D62A331F504F7E70B0B4A4E69C3ACD0E6EB11169D174D7C769ECB3B5FC24606D9F5879EB7DA954616A1D