Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_assertion description "[A decrease in CAD patients carrying the CAC haplotype compared to controls (p=0.043) and a decrease in the CAC haplotype in CAD patients with hypertension vs healthy controls (p=0.029) were demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_assertion evidence source_evidence_literature NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_assertion SIO_000772 19578791 NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_assertion wasDerivedFrom befree-20150227 NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_assertion wasGeneratedBy ECO_0000203 NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP276517.RAWlww3hr1OwHOQMvc7tEClDefj6S-eFPRTSt2XtUqPTg130_provenance.