Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_assertion description "[Our data supports the hypothesis that 5-HT(3) receptors play an important role in the pathogenesis of CINV. Along with previously identified HTR3 polymorphisms, the HTR3D p.G36A variant could also contribute to facilitating individual risk predictions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_assertion evidence source_evidence_literature NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_assertion SIO_000772 20602613 NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_assertion wasDerivedFrom gad-20150221 NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_assertion wasGeneratedBy ECO_0000203 NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180559.RAwnRIio83Xb9hqET2G6pPEPrJ9M3PwN8yE0Q3YU3YnJY130_provenance.