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- source_evidence_literature type ECO_0000212 NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_assertion description "[Mutations in the Factor H gene are associated with severe and diverse diseases including the rare renal disorders hemolytic uremic syndrome (HUS) and membranoproliferative glomerulonephritis (MPGN) also termed dense deposit disease (DDD), as well as the more frequent retinal disease age related macular degeneration (AMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_assertion evidence source_evidence_literature NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_assertion SIO_000772 19388168 NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_assertion wasDerivedFrom befree-2016 NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_assertion wasGeneratedBy ECO_0000203 NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.
- befree-2016 importedOn "2016-02-19" NP734263.RAVEN2HVTmkf7Lr-8csdcWOr4Qopd0wmyWORS5dEuBW0U130_provenance.