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DESCRIBE <http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82>
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http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82
http://www.w3.org/2000/01/rdf-schema#comment
"there is a spectrum of both prevalent and rare mutations that collectively have a significant impact on susceptibility to atopic disease"
xsd:string
http://purl.uniprot.org/uniprot/#_E9ADCE37176949ABFBD04CDB08AAE9B0A6FB1B24BE6DBF2B8203D7262BF8D022C90761C9F2DA5F7E99C189811B80093A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82
http://purl.uniprot.org/uniprot/Q01212
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82
http://purl.uniprot.org/uniprot/#_Q01212-mappedCitation-17502856
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A8EE61FE96162DB05B155252B9790C846AAD3854837696B3830B4399F572B132D3A03845A7A3F40B419049FB82896D82