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DESCRIBE <http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894>
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http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894
http://www.w3.org/2000/01/rdf-schema#comment
"Molecular analysis showed that the patient of alexander's disease was a heterozygote of the L331P mutation of GFAP."
xsd:string
http://purl.uniprot.org/uniprot/#_ADC16F53FE2A9419C599C7E4992E546F6B088E339382E98F83CD13A21C07E019F7D812F8E6B7A8643797DA0CFB0AE154
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894
http://purl.uniprot.org/uniprot/A0A224AME3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894
http://purl.uniprot.org/uniprot/#_A0A224AME3-mappedCitation-15465095
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B7B7DC441EBC599DF89BEFD44C389DC335E5A0A6B9BCA4D4A4B71CF554B8A8B83056513F261522D945DBA02765EE9894