Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_assertion description "[NS3 mutants lacking the helicase domain retained the ability to control virus signaling initiated by retinoic acid-inducible gene-I (RIG-I) or melanoma differentiation antigen 5 and suppressed the downstream activation of interferon regulatory factor-3 (IRF-3) and nuclear factor kappaB (NF-kappaB) through the targeted proteolysis of IPS-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_assertion evidence source_evidence_literature NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_assertion SIO_000772 17289677 NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_assertion wasDerivedFrom befree-2016 NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_assertion wasGeneratedBy ECO_0000203 NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.
- befree-2016 importedOn "2016-02-19" NP592994.RARtqAp6Epi06tgJWTzDqp4VThvh_GMx0nM8uP7CC0eis130_provenance.