Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion> ?p ?o ?g. }
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- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion type Assertion NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_head.
- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_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." NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_provenance.
- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion evidence source_evidence_literature NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_provenance.
- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion SIO_000772 14615367 NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_provenance.
- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion wasDerivedFrom gad-20150221 NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_provenance.
- NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_assertion wasGeneratedBy ECO_0000203 NP61972.RAK941lbuiIL4UoSZsiHQfFm3TIX9JwFd-mLCmYfdoH1E130_provenance.