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DESCRIBE <http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2>
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http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2
http://www.w3.org/2000/01/rdf-schema#comment
"Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H)."
xsd:string
http://purl.uniprot.org/uniprot/#_D25C1ACE3F6462F2CD223DA4490BF8C0B561083AE6FE7CB4DB0E711FF44D2BAB8707A077A6CE5A7C18BA1F804AE18908
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2
http://purl.uniprot.org/uniprot/B7Z6P1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2
http://purl.uniprot.org/uniprot/#_B7Z6P1-mappedCitation-18461503
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C925000F2E1F1FB41B4A9CE46DF4DD82D7CCBD786917235DE6A4C68332691E1C32F35C2908496CB144DADAF78CB3C2F2