Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_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." NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_assertion evidence source_evidence_literature NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_assertion SIO_000772 14615367 NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_assertion wasDerivedFrom befree-20150227 NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_assertion wasGeneratedBy ECO_0000203 NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP496002.RA3kCFk_J9srsxGQ8CPsGOwGF7KtxuewqAQgrH7wKRcc8130_provenance.