Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_assertion wasGeneratedBy ECO_0000203 NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_assertion wasDerivedFrom gad-20130706 NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_assertion SIO_000772 15327835 NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_assertion evidence source_evidence_literature NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_assertion description "[We compared the frequencies of polymorphisms in ten genes that have been hypothesized to have a role in risk of EC (CYP1A1, CYP2A6, CYP2E1, GSTM1, GSTP1, GSTT1, ADH2, ADH3, ALDH2, and O6-MGMT) among three Iranian ethnic groups with highly varying rates of EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP45663.RALMFfm7NpTKrvCkj0mn9zDYfVaSjyAgo6t9jPZNw9LuU130_provenance.