Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_assertion description "[Polymorphic variation in ALDH2, XPD and MGMT genes may be of importance for ESCC susceptibility. Polymorphic variation in CYP2A6 and MGMT are associated with ESCC metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_assertion evidence source_evidence_literature NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_assertion SIO_000772 20128036 NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_assertion wasDerivedFrom gad-20150221 NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_assertion wasGeneratedBy ECO_0000203 NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP112976.RAVjEV8CuzJRtjk0WrH_6umzBMR2LmUXUi2AsRFYtHfYw130_provenance.