Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_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." NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_assertion evidence source_evidence_literature NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_assertion SIO_000772 19238116 NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_assertion wasDerivedFrom befree-20140225 NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_assertion wasGeneratedBy ECO_0000203 NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP359699.RAMJgxAHv4zoDGQq8UVq2JT39gHYGBBeIUeYANSYQcIpw130_provenance.