Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_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." NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_assertion evidence source_evidence_curated NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_assertion SIO_000772 21572414 NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_assertion wasDerivedFrom ctd_human-20130708 NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_assertion wasGeneratedBy ECO_0000218 NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP23778.RAW4mZvqqEjn3O_O6LNOacLSeMOmWKZsFBMLDO4aGP1c8130_provenance.