Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_assertion description "[A prospective population-based study of CKD risk was conducted among 3706 black individuals without severe renal dysfunction at baseline (serum creatinine > or =177 micromol/L [2.0 mg/dl] for men, > or =159 micromol/L [1.8 mg/dl] for women) to examine associations with AGT and AT1R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_assertion evidence source_evidence_literature NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_assertion SIO_000772 16396964 NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_assertion wasDerivedFrom befree-2016 NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_assertion wasGeneratedBy ECO_0000203 NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.
- befree-2016 importedOn "2016-02-19" NP529709.RA-p-CDFSyldoJ3sLypny8skeW-F9HMsTpB1rbtikYRsA130_provenance.