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DESCRIBE <http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D>
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http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D
http://www.w3.org/2000/01/rdf-schema#comment
"Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1)."
xsd:string
http://purl.uniprot.org/uniprot/#_7CFFC3EAA9188242A979D3DF80B7643D0FECB65A2B3B21AE3DC98600D8DD32D079210C09CE96B2F19E85334017E3D439
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D
http://purl.uniprot.org/uniprot/B4DNJ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D
http://purl.uniprot.org/uniprot/#_B4DNJ7-mappedCitation-32821486
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F4C3222BD40579BF7CC40E94F6490E372F68F0D794077822DA1A48DE931A7397CC2904E5CDDADDE55BB6ADD4A3FFB59D