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DESCRIBE <http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914>
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http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914
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/#_8F5BF5097050E910DEB43C93C5293CF173FCE7DBE67FC19EBA64638D565992C7689F3DA988B16204EF87D013F80FB791
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914
http://purl.uniprot.org/uniprot/D0EKE4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914
http://purl.uniprot.org/uniprot/#_D0EKE4-mappedCitation-24025584
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/71D498BE76AACE89B3FE26A54FB42751AE58960261F80498BA3EFFD0CBF5C160B6E981C46528B291B979694571E93914