Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_assertion description "[The highest risk of meningioma was associated with heterozygosity for both MTHFR variants odds ratio (OR), 2.11; 95% confidence interval (95% CI), 1.42-3.12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_assertion evidence source_evidence_literature NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_assertion SIO_000772 18483342 NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_assertion wasDerivedFrom gad-20150221 NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_assertion wasGeneratedBy ECO_0000203 NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123116.RAf0mJgGeG66VKFi_rZtBOwKFrcnJnTmDldbo8Ux870lk130_provenance.