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DESCRIBE <http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C>
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http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C
http://www.w3.org/2000/01/rdf-schema#comment
"The GNAS mutation was specifically found in the cases with IPMN and it was speculated that some PDACs might be influenced by the concomitant but separately-located IPMN in their pathogenic mechanism."
xsd:string
http://purl.uniprot.org/uniprot/#_851B1A73AC786B8615554A83A26894D240A786E950DECAE3F9FFBFE2293EAAE1B680FF323DB8C325E2FBFFFBAC082CF2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C
http://purl.uniprot.org/uniprot/A0A7I2V5R6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C
http://purl.uniprot.org/uniprot/#_A0A7I2V5R6-mappedCitation-24897499
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/24461C439ACA1DEBB6F64299094FED4FB2A3B9C0C67CB607CA80158F8AD07FB79C0B111C2DDED6853C6C4816E808D06C