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DESCRIBE <http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA>
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http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA
http://www.w3.org/2000/01/rdf-schema#comment
"Our unique case report provides new data for what appears to be a new phenotype for AIP mutation-positive patients: apoplexy and consequently pituitary deficiency (rather than hormone excess)."
xsd:string
http://purl.uniprot.org/uniprot/#_D540AD9A4D10FA1E25C1B62CCB72473A0CE2521DC2E2930AA9C5D37B043E7D698C285A9A9B51DB279FEFFFCC38EAE6EF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA
http://purl.uniprot.org/uniprot/D5LTB3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA
http://purl.uniprot.org/uniprot/#_D5LTB3-mappedCitation-24025584
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/ACC72722E922F41357E97298EE2782B8C3292ADC7E2233608F8E4E1FE2A36272AA908479971C76AB9B50086F545287FA