Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_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." NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_assertion evidence source_evidence_literature NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_assertion SIO_000772 21978756 NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_assertion wasDerivedFrom befree-20150227 NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_assertion wasGeneratedBy ECO_0000203 NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP770804.RASq55UzlFdvNqh9UmTc0LmOeDbob1cCin0UHf6pkGpWQ130_provenance.