Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_assertion description "[ACE genotype was I/I, I/D and D/D in none, 12 and five patients, respectively, with minimal change glomerulopathy, and in one, five and two patients, respectively, with focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_assertion evidence source_evidence_literature NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_assertion SIO_000772 17199794 NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_assertion wasDerivedFrom gad-20150221 NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_assertion wasGeneratedBy ECO_0000203 NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP104726.RAgoCEs_ENTWjSAJOYIUWH8GwnEwHwxrbQfUyeHM0UELo130_provenance.