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DESCRIBE <http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286>
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http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286
http://www.w3.org/2000/01/rdf-schema#comment
"Molecular diagnostics for DNAJC12 variants are thus mandatory in all patients in which deficiencies of PAH and BH4 are genetically excluded."
xsd:string
http://purl.uniprot.org/uniprot/#_C6C6EEAE3E90926BAFE1D052FE099DE1863B03475FCC61152E090D968B14611A2BDD87110241C83C90C28C4A231CB2DB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286
http://purl.uniprot.org/uniprot/P00439
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286
http://purl.uniprot.org/uniprot/#_P00439-mappedCitation-29174366
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F5BA2079FAF1D0B134DB6EE635CFEDE4938D7A2EB0CBF214E9AAB05540A29AF83DF2BA5DC617F93EF8212A1426396286