Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_assertion description "[We examined whether the M235T polymorphism of the angiotensinogen (AGT) gene, the insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE) gene, and the A1166--> C polymorphism of the angiotensin II type 1 receptor gene may be associated with disease progression in 168 Caucasian patients with IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_assertion evidence source_evidence_curated NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_assertion SIO_000772 9259580 NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_assertion wasDerivedFrom ctd_human-20130708 NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_assertion wasGeneratedBy ECO_0000218 NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8062.RA9PSzKY_vINZe_QYPgGcSIpf2dCmbXMsVOI7ZIc2EHzk130_provenance.