Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_assertion description "[Finally, we have not proved any significant influence of the polymorphisms at positions -2578 C/A and -1154 G/A of the vascular endothelial growth factor gene promoter on the progression of chronic glomerulonephritides even though our study suggests a negative effect of CC genotype of -2578 C/A polymorphism on the clinical course of minimal change disease/focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_assertion evidence source_evidence_literature NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_assertion SIO_000772 21978756 NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_assertion wasDerivedFrom befree-20140225 NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_assertion wasGeneratedBy ECO_0000203 NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197213.RAoJzxWDTxSWfaVPuv9UXuywwUaIziDonyxBB8R4nKrlA130_provenance.