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DESCRIBE <http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7>
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http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); Patients carrying a variant low-activity NQO1 allele had a significantly increased risk of developing a SMN. The observed effect was restricted to solid tumors"
xsd:string
http://purl.uniprot.org/uniprot/#_15AE86BFD4EC1A56E0E2291B4E217D6E77C01ADAB98EEB36701A86BD58D3F367644AC3FD162EC4A68A33E08400B31E5A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7
http://purl.uniprot.org/uniprot/B4DLR8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7
http://purl.uniprot.org/uniprot/#_B4DLR8-mappedCitation-18024413
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CC3340E0EC78BDED144119BDD68F8FEC9201DA8B8B09BD50CC3310D1A261F92D0F82F4341D0096D4F248C75AA4765BF7