Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion> ?p ?o ?g. }
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- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion type Assertion NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_head.
- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_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." NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_provenance.
- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion evidence source_evidence_literature NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_provenance.
- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion SIO_000772 19388168 NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_provenance.
- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion wasDerivedFrom befree-2016 NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_provenance.
- NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_assertion wasGeneratedBy ECO_0000203 NP734266.RAGFB6ZG02hfV6UicaX33DcJ_ohZuI0TJzDCaZb-ADGwI130_provenance.