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- source_evidence_literature type ECO_0000212 NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_assertion description "[This study emphasizes that modifiers such as CD46 and FHL-1 may determine the kidney phenotype of patients who present with homozygous CFH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_assertion evidence source_evidence_literature NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_assertion SIO_000772 23870792 NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_assertion wasDerivedFrom befree-20140225 NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_assertion wasGeneratedBy ECO_0000203 NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP666723.RAf71chQlQhHoPp6MtDQMtDijZ7o3Ez8nPY2B0mOoXdRw130_provenance.