Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_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." NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_assertion evidence source_evidence_literature NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_assertion SIO_000772 18385087 NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_assertion wasDerivedFrom befree-20140225 NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_assertion wasGeneratedBy ECO_0000203 NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP396718.RAJCx0CLG0PBKwdaSJEF2Kb937nucmh-7I5h3P_Dr9YAA130_provenance.