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DESCRIBE <http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5>
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http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5
http://www.w3.org/2000/01/rdf-schema#comment
"XLID syndrome gene Med12 promotes Ig isotype switching through chromatin modification and enhancer RNA regulation."
xsd:string
http://purl.uniprot.org/uniprot/#_4848B6687DCF411E1AF8A4B987C1FF9B5DAFCF46BAE04B037B148FE7E5466D20434331944DF8ECCFE5B6B2B4FCE15E33
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5
http://purl.uniprot.org/uniprot/Q93074
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5
http://purl.uniprot.org/uniprot/#_Q93074-mappedCitation-36427307
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CDD680BEB1000E12D146B4FD54BC4F9BF2C4FA50BB2C384BEBB1A699EE5BF57FDC9C3EEFF6C1B76FB79F57A21CFD73B5