Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_assertion description "[Although borderline support for association between polymorphisms in TLR genes and AMD was reported for some cohorts, these initial observations of coding SNPs in TLR3, TLR4, and TLR7 were not replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_assertion evidence source_evidence_literature NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_assertion SIO_000772 18385087 NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_assertion wasDerivedFrom gad-20150221 NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_assertion wasGeneratedBy ECO_0000203 NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122496.RAQJgrsdgIYFHWS_mPlzWY7B4SSe2BH8gSRA6rFG0ye6U130_provenance.