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DESCRIBE <http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0>
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http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0
http://www.w3.org/2000/01/rdf-schema#comment
"There are no significant differences between PEX1- PEX6- and PEX26-associated phenotypes inclinical and genetic spectrum of Heimler syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_9DE68FF9B0B38ACDCACB37C769D92E97B82BCF75030B5363673849783E39DA7EAC02BE92D6D664194E46862E80B35F5C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0
http://purl.uniprot.org/uniprot/A0A024R100
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0
http://purl.uniprot.org/uniprot/#_A0A024R100-mappedCitation-31831025
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E37A39AA10F2464C095718F75B558A37BD909DB812B1EC380ABED9176B3E4CEB7B63E327CCBA566D3008198D2F1535F0