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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF>
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http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF
http://www.w3.org/2000/01/rdf-schema#comment
"SOX3 duplication is a genetic cause for XH but has incomplete penetrance. Moreover increased SOX3 levels may be a risk factor for NTD and potentially other clinical characteristics."
xsd:string
http://purl.uniprot.org/uniprot/#_C4C1D3E718CC5E59D6CA6704E46858BF22C851665005322E635BFD5B9810E59FD458ED09AD311BF6E57C7EF708851094
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF
http://purl.uniprot.org/uniprot/Q15505
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF
http://purl.uniprot.org/uniprot/#_Q15505-mappedCitation-24737742
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A3A85CC2EBF5510360B6B1B41A94D925108368771D16EC1B29356705F1E7804154C94825C0410CC3CF4B7F5C789F94AF