Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_assertion description "[Results showed that ADH1B (rs1229984) was associated with EC with odds ratios (ORs) of 1.34 [95% confidence interval (CI): 1.08-1.66] for G-allele carriers compared to A/A homozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_assertion evidence source_evidence_literature NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_assertion SIO_000772 22930414 NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_assertion wasDerivedFrom befree-20140225 NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_assertion wasGeneratedBy ECO_0000203 NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434808.RARnZnQbLwKw2o9-2m_8VwAgfklYm4NFhog_Buax-sSUU130_provenance.