Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_assertion description "[We conclude that the mutated genotypes of the ScaI polymorphism are negatively associated with overt nephropathy, whereas the mutated genotypes of BstXI polymorphism are positively associated with microalbuminuria. hANP gene variants may exert a protecti]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_assertion evidence source_evidence_literature NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_assertion SIO_000772 11408388 NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_assertion wasDerivedFrom gad-20150221 NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_assertion wasGeneratedBy ECO_0000203 NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67381.RACUog_POzFzPxSF1vsR9dLC4qzglJJZ8A9ZLegwxMLCQ130_provenance.