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DESCRIBE <http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3>
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http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3
http://www.w3.org/2000/01/rdf-schema#comment
"Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease."
xsd:string
http://purl.uniprot.org/uniprot/#_CFF38039355E74155417266A4F8F74848CF5B1B09348A16349D0992629F4F888E67416D98E271B2B1C023637D7B335AC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3
http://purl.uniprot.org/uniprot/Q9H0U3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3
http://purl.uniprot.org/uniprot/#_Q9H0U3-mappedCitation-35264785
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E510CF4FB9215EBE13EEA97E04384A3E12EA630E1E8312D7D4378EC4428A7B711F993BF4E7820D45DE2C3093224846C3