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DESCRIBE <http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3>
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http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3
http://www.w3.org/2000/01/rdf-schema#comment
"interference with the binding of Hexokinase-I to mitochondria by VDAC1-derived peptides may offer a novel strategy by which to potentiate the efficacy of conventional chemotherapeutic agents"
xsd:string
http://purl.uniprot.org/uniprot/#_D2173BC3DD309B674B9C1374B8CDB0E2424FB79463BAB65FB86897C2E0BD2FADA86ACC599BE6F2F05F91850C55EED818
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3
http://purl.uniprot.org/uniprot/B4DG62
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3
http://purl.uniprot.org/uniprot/#_B4DG62-mappedCitation-18308720
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/84E51373BB12FD042D5831D363B68D3636C86B85AC97D0BBC0CC74CDFAF3144A2690F12E206CF2F74678CF06CEB8BDD3