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DESCRIBE <http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687>
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http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687
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/#_B8BFB1B562ED4A55C49252D0513205D184FB8E0653F8C6C7AABD8B14C7F5F1EA58A5ADF9EA8DF891E8F43BB22F7CB125
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687
http://purl.uniprot.org/uniprot/Q16021
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687
http://purl.uniprot.org/uniprot/#_Q16021-mappedCitation-29174366
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F05F00CF427F9CE772FF29D3845BAE69112178711766D55D30CEB94786BF83FB44EBF114AA73B931CE0674CC1F143687