Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_assertion description "[We concluded that AGT and AT1 polymorphisms are independent genetic risk factors for lacunar infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_assertion evidence source_evidence_literature NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_assertion SIO_000772 10701810 NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_assertion wasDerivedFrom befree-20140225 NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_assertion wasGeneratedBy ECO_0000203 NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP215633.RAuHbx8vL8C7BoJVjC3GC2wCL9UH9NwRAkCVTyXlJJRnw130_provenance.