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DESCRIBE <http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A>
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http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A
http://www.w3.org/2000/01/rdf-schema#comment
"two novel mutations each causing a premature stop codon - a genetic basis for TC I deficiency"
xsd:string
http://purl.uniprot.org/uniprot/#_73E0DDC18F17D6800DF32E8F0BCA61776C874E62A6529361702DDA9CD02C3F1920B52259BD9142AF4A6156D38DAFDC93
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A
http://purl.uniprot.org/uniprot/P20061
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A
http://purl.uniprot.org/uniprot/#_P20061-mappedCitation-19686235
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/23B9DF993224E7F86A5D2D3DA52236C914970CF87454098DCEDAAD28DB70ECEE760EBD742FE66ECCFC088BFD3D38EE3A