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DESCRIBE <http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841>
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http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841
http://www.w3.org/2000/01/rdf-schema#comment
"Severe phenotype in 6 children with massive expansion of spinocerebellar ataxia type 2 may be due to a functional deficit in ATXN2 networks in the postsynapse."
xsd:string
http://purl.uniprot.org/uniprot/#_F1EE05C505687052724ECCF29D312FC94225D240E83EA0082B26F3E8EC4CD7D074F2651AAF771EF6812EE202B73A8608
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841
http://purl.uniprot.org/uniprot/Q2M2R5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841
http://purl.uniprot.org/uniprot/#_Q2M2R5-mappedCitation-21880993
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/907EF1EAAF30CD3F9AA4C0D1A9EE83F78CEA934680F4A4474B11B7571D2AABD1990F35385285E8382ED4C3BF2FAB3841