Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion> ?p ?o ?g. }
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- NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion type Assertion NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_head.
- 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.