Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_assertion description "[The combination of TNF (-308)GG homozygosity and the IL4R 503P variant carrier status was associated with a particularly strong predisposition to LV stroke (odds ratio [OR] = 5.5; 95% confidence interval [CI] = 2.3-13.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_assertion evidence source_evidence_literature NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_assertion SIO_000772 14615367 NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_assertion wasDerivedFrom befree-20140225 NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_assertion wasGeneratedBy ECO_0000203 NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP568531.RAiyWzWLwsM1RocHZXdAquEaSm0VTBNwyaGvNBNxgW2FM130_provenance.