Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_assertion description "[Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_assertion evidence source_evidence_curated NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_assertion SIO_000772 14978182 NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_assertion wasDerivedFrom ctd_human-20150221 NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_assertion wasGeneratedBy ECO_0000218 NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP10186.RAzhG4_R1dRw07pW5AjYD6-_hba1MPELlht2ttZ2cdndw130_provenance.