Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_assertion description "[Polymorphic variations in the MTR, SLC19A1, and TYMS genes were associated with better clinical response to combination DMARD regimens containing MTX and SSZ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_assertion evidence source_evidence_literature NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_assertion SIO_000772 18322994 NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_assertion wasDerivedFrom gad-20150221 NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_assertion wasGeneratedBy ECO_0000203 NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP80405.RAfGOqmTOC3ZG43EJjDSYfNQ6CktuW6aejmsimlOKwRd8130_provenance.