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DESCRIBE <http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA>
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http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA
http://www.w3.org/2000/01/rdf-schema#comment
"a novel and rare 1 bp insertion/nonsense mutation c1378_1379insG (exon 12) and the entire deletion of exon 7 in early-onset Parkinson's disease."
xsd:string
http://purl.uniprot.org/uniprot/#_572683B80F6842824FA73905FE03A7703785A3D53E2E7F3C5B054B91C0869D301BDEFF228D4F974C4F69755806D9BF90
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA
http://purl.uniprot.org/uniprot/A0A1W5XGE1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA
http://purl.uniprot.org/uniprot/#_A0A1W5XGE1-mappedCitation-18188499
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7DAE2C295071BD62D6A7DD1CA63223ADF29946BEE733B3737160AB5FF0F2CCAE5E3FCCC7E1FCC9C41AA12B8CC9FA2DAA