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DESCRIBE <http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD>
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http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD
http://www.w3.org/2000/01/rdf-schema#comment
"Thus it seems unlikely that DYX1C1 gene would be involved in the genetic etiology of autism in Finnish patients."
xsd:string
http://purl.uniprot.org/uniprot/#_909945D7F4C5F0EC8983F56AC0F354043E539B385E9800B5C9C40FFB2267ABF431324F326E12CC026E8E4DC6F634B526
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD
http://purl.uniprot.org/uniprot/B4DY92
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD
http://purl.uniprot.org/uniprot/#_B4DY92-mappedCitation-15470369
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2C2F612D13B8C1F3D69778C8BB06CB0DC52397297354F993BB086CCC59193004CF5197730EE690725565CB963B7231CD