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- source_evidence_literature type ECO_0000212 NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_assertion description "[We found that: (i) genotypes, including those of APOA5 S19W, APOA5 -1131T > C, APOE, GCKR, TRIB1 and TBL2/MLXIPL, were significantly associated with severe HTG; (ii) odds ratios for these genetic variables were significant in both univariate and multivariate regression analyses, irrespective of the presence or absence of diabetes or obesity; (iii) a significant fraction-about one-quarter-of the explained variation in disease status was associated with these genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_assertion evidence source_evidence_literature NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_assertion SIO_000772 18596051 NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_assertion wasDerivedFrom befree-2016 NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_assertion wasGeneratedBy ECO_0000203 NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.
- befree-2016 importedOn "2016-02-19" NP679915.RA1BsB66S4ScTODE1E_1P_NgXWNRsZvIuUuTG8yAHoHyo130_provenance.