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- source_evidence_literature type ECO_0000212 NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_assertion description "[Only the ACE gene polymorphism showed evidence of association with albuminuria, with the D allele being less frequent in the normoglycemic hypertensive patients with albuminuria (25.0%) than the controls (41.4%) or normoalbuminuric group (39.6%) and in those hypertensives at increased risk (albumin-to-creatinine ratio > 5.6 mg/mmol) of end-stage renal disease than those at lower risk (all p < 0.05), but not in the diabetic group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_assertion evidence source_evidence_literature NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_assertion SIO_000772 11200871 NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_assertion wasDerivedFrom befree-20140225 NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_assertion wasGeneratedBy ECO_0000203 NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP684392.RAPn8fgj5Co2gLutYBKiR4lI86f0x89WHLOFz3OsbkIVI130_provenance.