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DESCRIBE <http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021>
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http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021
http://www.w3.org/2000/01/rdf-schema#comment
"Identify CH5424802 as a potent selective and orally available ALK inhibitor with a unique chemical scaffold showing preferential antitumor activity against cancers with gene alterations of ALK."
xsd:string
http://purl.uniprot.org/uniprot/#_51A4D901F2C7645FE03F1734DA4D6295913191186703545511D1CE7968466AC7207557946E0490F53444FF7EF64CC97C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021
http://purl.uniprot.org/uniprot/B6D4Y2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021
http://purl.uniprot.org/uniprot/#_B6D4Y2-mappedCitation-21575866
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CF074BFBF26282DEF2F78FB6E7AF4434A7CE167E1C6791A6C10A2BB638DD09F765FC5C36272AAFF43F2D1926E358A021