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DESCRIBE <http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2>
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http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2
http://www.w3.org/2000/01/rdf-schema#comment
"A significant association of TNFRSF13B gene mutations was observed in common variable immunodeficiency patients."
xsd:string
http://purl.uniprot.org/uniprot/#_A4290C78CE9A83283AAC7C13162BC837752865112A37E41F05690B35158D93F7B3C22DD2D2DEC2FFA8267067B099D394
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2
http://purl.uniprot.org/uniprot/O14836
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2
http://purl.uniprot.org/uniprot/#_O14836-mappedCitation-22884984
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BC8E55030DAECAD50D68DD8FAFD52419044672CF87D6EFB3FBE7FC2B3B8043854BDE4F0E2F3EFD352D86FF2D7777FDB2