Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_assertion description "[This study investigated the genetic variants of four bilirubin metabolism genes--heme oxygenase-1 (HMOX1), biliverdin reductase A (BLVRA), solute carrier organic anion transporter family member 1B1 (SLCO1B1), and uridine diphosphate glycosyltransferase 1A1 (UGT1A1)--in relation to TBIL levels and CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_assertion evidence source_evidence_literature NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_assertion SIO_000772 19238116 NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_assertion wasDerivedFrom gad-20150221 NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_assertion wasGeneratedBy ECO_0000203 NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP141608.RA09OEOvHIn8wCoPYXjMr7rXNV1ML5NaSjwAT-rkObe3M130_provenance.