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- source_evidence_literature type ECO_0000212 NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_assertion description "[In conclusion, our findings indicate that the observed association of TAP variants with IDDM in German patients is due to linkage disequilibrium with HLA DQ alleles/DRB1*04 subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_assertion evidence source_evidence_literature NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_assertion SIO_000772 9226129 NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_assertion wasDerivedFrom befree-2016 NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_assertion wasGeneratedBy ECO_0000203 NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1376983.RAB3jzbidY4M5MtUN__hWb5pG55BbBf8eXgtxSrCwlZN4130_provenance.