Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_assertion description "[Monogenic mutations leading to excessive activation of the mineralocorticoid pathway result, almost always, in suppressed renin and hypertension in adult life and sometimes in hypokalaemia and alkalosis, which can be severe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_assertion evidence source_evidence_literature NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_assertion SIO_000772 16980202 NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_assertion wasDerivedFrom befree-20150227 NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_assertion wasGeneratedBy ECO_0000203 NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP669365.RA4PnHW5v-g4uRrgBag2nmR7Is0v6FKVJjRSG7qUR-sGI130_provenance.