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DESCRIBE <http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C>
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http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C
http://www.w3.org/2000/01/rdf-schema#comment
"Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy."
xsd:string
http://purl.uniprot.org/uniprot/#_996690D1DB46F7D7E6FE4504D699EBFE351DA40BA6A7368FD1FAA80E08606F19EA083966AEF64E436E76E1621D080DB6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C
http://purl.uniprot.org/uniprot/Q56R94
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C
http://purl.uniprot.org/uniprot/#_Q56R94-mappedCitation-32994279
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0C68685FF66F318DCC47EAAB527F636281612D50090F908A6DFAE7871004C80D5147E5ABE0B97ED51BEA7E431602218C