Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_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." NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion evidence source_evidence_literature NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion SIO_000772 19388168 NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion wasDerivedFrom befree-20140225 NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion wasGeneratedBy ECO_0000203 NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance.