Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_assertion description "[We determined the B2BKR genotype of 90 patients with essential hypertension and echocardiographically diagnosed LV hypertrophy, included in a double-blind study to receive treatment for 48 weeks with either the angiotensin II type 1 (AT1) receptor antagonist irbesartan or the beta1-adrenoceptor antagonist atenolol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_assertion evidence source_evidence_literature NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_assertion SIO_000772 12640257 NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_assertion wasDerivedFrom befree-2016 NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_assertion wasGeneratedBy ECO_0000203 NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.
- befree-2016 importedOn "2016-02-19" NP387178.RAgpEp7J1tSPZbUnWLQuAeIDJyNJb_Bxd65a0P7lJiH-c130_provenance.