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- source_evidence_literature type ECO_0000212 NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_assertion wasGeneratedBy ECO_0000203 NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_assertion wasDerivedFrom befree-20150227 NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_assertion SIO_000772 10977777 NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_assertion evidence source_evidence_literature NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.
- NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_assertion description "[We performed an association study of patients with IgA nephropathy and matching control subjects to test whether the G38A polymorphism in the uteroglobin gene, the C2093T polymorphism in the megsin gene, or the angiotensin-converting enzyme (ACE) insertion/deletion polymorphism is associated with IgA nephropathy or rate of disease progression in patients with IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802269.RA3zj_vkP2Yf-eSsGqT2rqDqME73z-q2EBku9QD8JCqM4130_provenance.