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DESCRIBE <http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A>
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http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A
http://www.w3.org/2000/01/rdf-schema#comment
"Data sugget that inhibition of dUTPase is a mechanism-based therapeutic approach to significantly enhance the efficacy of thymidylate synthase (TS)-targeted chemotherapeutic agents."
xsd:string
http://purl.uniprot.org/uniprot/#_A65B9A06A25EFC365747F322C6B99023698B4D1E8E5336D5EA2A9D0FD7531476404E97D40EC88EF17E0E1FF8F35DEE1E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A
http://purl.uniprot.org/uniprot/Q53Y97
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A
http://purl.uniprot.org/uniprot/#_Q53Y97-mappedCitation-22172489
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B663F0C227EF17C4A8BD51ADC9BD4614C555A80303161EA58D97786B8EB2CA8588E20C0CCB27C35CF903BB3B4346615A