Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_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." NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_assertion evidence source_evidence_literature NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_assertion SIO_000772 18483342 NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_assertion wasDerivedFrom befree-20140225 NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_assertion wasGeneratedBy ECO_0000203 NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476087.RAH_N1IFJlj0UvnsyiMkJxnhs0ropAnYS55G-4eV7OJ9M130_provenance.