Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion description "[Bartter syndrome, an autosomal recessive renal tubular disorder, is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentrations with low or normal blood pressure and renal salt loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion evidence source_evidence_literature NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion SIO_000772 9502574 NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion wasDerivedFrom befree-20140225 NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion wasGeneratedBy ECO_0000203 NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance.