Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion> ?p ?o ?g. }
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- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion type Assertion NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_head.
- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion description "[Mutations in the CFH gene are associated with atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis type II and C3 glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_provenance.
- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion evidence source_evidence_literature NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_provenance.
- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion SIO_000772 21270828 NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_provenance.
- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion wasDerivedFrom befree-20140225 NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_provenance.
- NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_assertion wasGeneratedBy ECO_0000203 NP798277.RASa3K7UV3KI5j26G6Yli5v1Y_EMEAj36LfNbyw70YZWg130_provenance.