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http://purl.uniprot.org/SHA-384/CC4B2BC694796048270789950025D56D3DEEE2C04ADEC08CB4F4604366BF781901959BABB0F48823B658525DE26FEF8Bhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CC4B2BC694796048270789950025D56D3DEEE2C04ADEC08CB4F4604366BF781901959BABB0F48823B658525DE26FEF8Bhttp://www.w3.org/2000/01/rdf-schema#comment"Laboratory tests and direct sequencing of PROC and SERPINC1 were conducted for the patient and his family members. Coagulation tests revealed that the patient presented type I antithrombin deficiency combined with decreased protein C activity resulting from a small insertion mutation c.848_849insGATGT in SERPINC1 and a short deletion variant c.572_574delAGA in PROC."xsd:string
http://purl.uniprot.org/uniprot/#_EF9622E87D250CF7DC87E47C803D69889A2E50A6D8A8DAE1C5F64BB6D5BF633C7BC1776B2FD582235A8FDFFAA1DAC94Dhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/CC4B2BC694796048270789950025D56D3DEEE2C04ADEC08CB4F4604366BF781901959BABB0F48823B658525DE26FEF8B
http://purl.uniprot.org/uniprot/Q9UBW9http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CC4B2BC694796048270789950025D56D3DEEE2C04ADEC08CB4F4604366BF781901959BABB0F48823B658525DE26FEF8B
http://purl.uniprot.org/uniprot/#_Q9UBW9-mappedCitation-28861852http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CC4B2BC694796048270789950025D56D3DEEE2C04ADEC08CB4F4604366BF781901959BABB0F48823B658525DE26FEF8B