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DESCRIBE <http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB>
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http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB
http://www.w3.org/2000/01/rdf-schema#comment
"The homozygous SMN2 deletion (2 : 0) was statistically more frequent and associated with earlier onset age and severity of illness in Korean amyotrophic lateral sclerosis patients."
xsd:string
http://purl.uniprot.org/uniprot/#_B2724417AFE29A43631141FC3056A84905C9F8F2506A14F5709D8E4B70AE54C658F18EC08E31B35B3E32C1FE4187F6F8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB
http://purl.uniprot.org/uniprot/E7EQZ4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB
http://purl.uniprot.org/uniprot/#_E7EQZ4-mappedCitation-22187232
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D62FBE0D5E7D964D528DEF405B1FF675625241353DFC151AB6B01A514F56A88DDE1A7B3CFDD5E8E6B537486C869616AB