Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_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." NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_assertion evidence source_evidence_literature NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_assertion SIO_000772 20602613 NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_assertion wasDerivedFrom gad-20150221 NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_assertion wasGeneratedBy ECO_0000203 NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP102441.RAiXF2FA94DUrz1MmUNstSQDIo7Z9Qhx73cjd9mDEFem4130_provenance.