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DESCRIBE <http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D>
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http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); the present findings represent the first demonstration of relationships between the AD genetic risk factor CST3 B and global neurophysiological phenotype"
xsd:string
http://purl.uniprot.org/uniprot/#_072EE4E861A45CA552B3B2B1AE3734A7E159CDC3DE3EC6D3F140C454FB52B7933F1653FE2AFC8A925F4E99A3D30DB993
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D
http://purl.uniprot.org/uniprot/P01034
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D
http://purl.uniprot.org/uniprot/#_P01034-mappedCitation-16213753
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/ED023ECCAFC66A9C6F4717D402C4B850E8C314860761A8BF2BF3D5969C901D7F930FBDE5FB28B6802E767956E071311D