Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_assertion description "[Carriers of the APOE ?2 SNP had a significantly lower risk of CHD hazard ratio (HR) of 0.63 (95% confidence interval [CI]: 0.42-0.95), as did carriers of the APOC2 SNP rs5127 (HR = 0.72, 95% CI: 0.56-0.93), while carriers of APOC1 SNP rs4803770 had higher risk of CHD (HR = 1.36, 95% CI: 1.04-1.78) compared with noncarriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_assertion evidence source_evidence_literature NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_assertion SIO_000772 20498921 NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_assertion wasDerivedFrom befree-2016 NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_assertion wasGeneratedBy ECO_0000203 NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.
- befree-2016 importedOn "2016-02-19" NP814349.RANXl5XueIKRPtHDAOKqh68SXRFQmWShYEekiVcT_kVMg130_provenance.