Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_assertion description "[Variants at three of these loci have previously been linked with important clinical outcomes: SLC7A9 is a risk locus for chronic kidney disease, NAT2 for coronary artery disease and genotype-dependent response to drug toxicity, and SLC6A20 for iminoglycinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_assertion evidence source_evidence_curated NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_assertion SIO_000772 21572414 NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_assertion wasDerivedFrom ctd_human-20150221 NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_assertion wasGeneratedBy ECO_0000218 NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP30261.RAkSDgMtOPI-6wC7RRns4NcSlQo6-a7oNW1ICdSKs6Zpw130_provenance.