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DESCRIBE <http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB>
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http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB
http://www.w3.org/2000/01/rdf-schema#comment
"Genomewide linkage analysis combined with whole-exome sequencing revealed two different heterozygous mutations affecting Galpha11 as novel causes of autosomal dominant isolated hypoparathyroidism."
xsd:string
http://purl.uniprot.org/uniprot/#_457B486E8309C526E119E11509FDE04B8655079BEC0D27E9D4EF254B897955B5A139CFCE106E02226E0B94AC81884D19
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB
http://purl.uniprot.org/uniprot/Q59FM5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB
http://purl.uniprot.org/uniprot/#_Q59FM5-mappedCitation-23802536
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9B88EF021E0E7A447C6DB91A2B99CA16B696532C48041CE40018B4BA8C54F2C5FD240F2C2099A33483FE72B9935FADBB