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DESCRIBE <http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F>
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http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F
http://www.w3.org/2000/01/rdf-schema#comment
"that a single mutation in the DCTN1 gene recapitulates symptoms of Perry syndrome patients"
xsd:string
http://purl.uniprot.org/uniprot/#_F860549546CD4B583C6E4B688A29D2F8F2F067E9F01B0F257C2D1A06BA0F07A4D52C71734ECC12C9E91CBC5B3D1D2D6C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F
http://purl.uniprot.org/uniprot/E9Q3M3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F
http://purl.uniprot.org/uniprot/#_E9Q3M3-mappedCitation-29273399
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DE28A668BD64D88BE1267D4E0AF1490DC3F8757258551D70704EB7634A9828DAD0ABCCAC446CB6185BE88ED070BB2E9F