Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_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." NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_assertion evidence source_evidence_literature NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_assertion SIO_000772 14615367 NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_assertion wasDerivedFrom gad-20150221 NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_assertion wasGeneratedBy ECO_0000203 NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82519.RAuiZj7xDtaWkP_6dAVRZsxTIwLNAN0TNvFppVT5rEQ14130_provenance.