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DESCRIBE <http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B>
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http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B
http://www.w3.org/2000/01/rdf-schema#comment
"The linkage scan excluded the majority of known myopathy genes but one linkage peak included the gene GNE in which mutations cause autosomal recessive hereditary inclusion body myopathy type 2 (HIBM2)."
xsd:string
http://purl.uniprot.org/uniprot/#_88CC43B7DE4AEA0C9FA8240F2EFECA993CDFA3A19EF336B66FAD66363832DAD03779506A158DD53AF90AAF702BA2CBBC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B
http://purl.uniprot.org/uniprot/Q9Y223
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B
http://purl.uniprot.org/uniprot/#_Q9Y223-mappedCitation-21708040
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/97131D3757D16DBC064F3A6B7433B1336D65637F208605063FEA06EF94E74D6C443302E393579119EEB3A90E7DE4B55B