Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion> ?p ?o ?g. }
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- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion type Assertion NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_head.
- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion description "[We analysed a microsatellite polymorphism (variant lengths of a dinucleotide (AT)n repeat) within exon 3 of the CTLA-4 gene in the following groups: 21 English patients with non-associated Addison's disease, 18 with autoimmune polyglandular syndrome type 2 (APS2) and 173 healthy control subjects; 26 Norwegian patients with non-associated Addison's disease, 9 with autoimmune polyglandular syndrome type 1 (APS1), 17 with APS2 and 100 controls; 3 Finnish patients with non-associated Addison's disease, 5 with APS2 and 71 controls; 10 Estonian patients with non-associated Addison's disease, 2 with APS2 and 45 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_provenance.
- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion evidence source_evidence_literature NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_provenance.
- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion SIO_000772 10197076 NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_provenance.
- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion wasDerivedFrom befree-20140225 NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_provenance.
- NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_assertion wasGeneratedBy ECO_0000203 NP607121.RAuxXnmvu1R2MU7PH-oSPKCKM9-y6AI_4Ep4H7Qd3cwaE130_provenance.