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DESCRIBE <http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3>
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http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3
http://www.w3.org/2000/01/rdf-schema#comment
"Such a complex diagnostic genetic profile has not been reported in ALK fusion-positive NSCLC. This case highlights the utility of comprehensive molecular testing in the diagnosis of NSCLC."
xsd:string
http://purl.uniprot.org/uniprot/#_28945C5B9AFA20653D2D9BDD717303D9E049CA5A7E7C0375435F6871F3B7FE5D47C4085425A9AAC9EB6B4AE0934C6C54
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3
http://purl.uniprot.org/uniprot/B6D4Y6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3
http://purl.uniprot.org/uniprot/#_B6D4Y6-mappedCitation-25964588
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/74A1A884CB97822B9211BACF74FF7AA4749AFA778ACD6EEEE44DE6F7079D3F53C48C2517536628BEE09CFBFB584D47C3