Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_assertion description "[We evaluated the relation between the ScaI and BstXI polymorphisms of the human ANP (hANP) gene, hypertension, and albuminuria in a clinical cohort of 1033 subjects, including type 1 and type 2 diabetic patients, nondiabetic subjects with essential hypertension, and nondiabetic normotensive control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_assertion evidence source_evidence_literature NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_assertion SIO_000772 11408388 NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_assertion wasDerivedFrom gad-20150221 NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_assertion wasGeneratedBy ECO_0000203 NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67386.RAV3kKo0MKMc6gX0PfDwFuqGAYdTXF9RoE0kGgAfJEzL0130_provenance.