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- source_evidence_literature type ECO_0000212 NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_assertion description "[Several recent studies have described the association of genetic variations of the complement factor H gene (CFH) with atypical haemolytic uraemic syndrome (aHUS), age-related macular degeneration (AMD) and membranoproliferative glomerulonephritis (MPGN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_assertion evidence source_evidence_literature NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_assertion SIO_000772 18081690 NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_assertion wasDerivedFrom befree-2016 NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_assertion wasGeneratedBy ECO_0000203 NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.
- befree-2016 importedOn "2016-02-19" NP645342.RAdHv36GY4aF3L_CoHjeo-HTONe2Q2H2JtPxiTRGlM_QI130_provenance.