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DESCRIBE <http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD>
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http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD
http://www.w3.org/2000/01/rdf-schema#comment
"Our results support the association of the +1858T risk allele of the +1858C/T PTPN22 polymorphism with susceptibility to RA and confirm that this SNP influence the autoimmune processes towards a development of RA in Mexican population."
xsd:string
http://purl.uniprot.org/uniprot/#_F0F5E7E861828AB02A9665ED930FEE8E81052B6A2423819943EB7C95519CF8C0A9D72A839EB101D942B0180B475AE254
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD
http://purl.uniprot.org/uniprot/A0A1S6KJG4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD
http://purl.uniprot.org/uniprot/#_A0A1S6KJG4-mappedCitation-22743847
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7CFB54D3743EFBB5EEB8E296947EC80F47E017990469DAAF8FC3F9BAE96917771FEB21714DBAE5B747D32EA24424B6AD