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- source_evidence_literature type ECO_0000212 NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_assertion description "[In a registry-based group of 525 recent-onset IDDM patients <40 years old we investigated the possible interactions of a CTLA-4 gene A-to-G transition polymorphism with age at clinical disease onset and with the presence or absence of established genetic (HLA-DQ, INS VNTR) and immune disease markers (autoantibodies against islet cell cytoplasm (ICA); insulin (IAA); glutamate decarboxylase (GAD65-Ab); IA-2 protein tyrosine phosphatase (IA-2-Ab)) determined within the first week of insulin treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_assertion evidence source_evidence_literature NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_assertion SIO_000772 9353155 NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_assertion wasDerivedFrom befree-2016 NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_assertion wasGeneratedBy ECO_0000203 NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1383036.RAf4g4_L7toZ1ckTotkTEO_J6JkeWz2EV27U1HyTcscNQ130_provenance.