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DESCRIBE <http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9>
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http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9
http://www.w3.org/2000/01/rdf-schema#comment
"A model for the functional defect in Erv1 R182H which could potentially be extended to human ALR R194H and provides insights into the molecular basis of autosomal recessive myopathy."
xsd:string
http://purl.uniprot.org/uniprot/#_3E2F485F82CCD042E105967AB3387F78CD838A2114A0CCB622C833AC81B35D739B4CAE927D9F0A8753EBF2AF9F5CC02B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9
http://purl.uniprot.org/uniprot/Q9H2X5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9
http://purl.uniprot.org/uniprot/#_Q9H2X5-mappedCitation-25269795
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BAA0808302DAACF1569E06F66CB65AF83E2701885C08BA33AB8DA680D45E482E1C8FC3996E234C3CEC2F16003E0D60D9