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DESCRIBE <http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2>
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http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2
http://www.w3.org/2000/01/rdf-schema#comment
"replication confirmed at genome-wide significance the association of loci at FOXE1 with hypothyroidism and PDE8B CAPZB and PDE10A with serum TSH. A total of 12 SNPs seemed to explain nearly 7% of the serum TSH variation"
xsd:string
http://purl.uniprot.org/uniprot/#_2AFE0B200EEB5EA40BC44B295EE97D2A79877C8E6A53180C4D6C1BC85E85E4AD20E1A191EFDAF736DE028443713834DE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2
http://purl.uniprot.org/uniprot/Q6GZ70
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2
http://purl.uniprot.org/uniprot/#_Q6GZ70-mappedCitation-28777242
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/47B5B1417B87176BC9AD91BF0803333EEBD98F081B156207265048594760384A30D16476BEA595ECF8CA058C85432FE2