Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_assertion description "[Frequencies of ADA*2 carriers (5.9% vs. 13.5%, p = 0.015) and ADA*2 allele (2.9% vs. 7.3%, p = 0.0083) were lower in CAD patients than in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_assertion evidence source_evidence_literature NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_assertion SIO_000772 17287605 NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_assertion wasDerivedFrom gad-20130706 NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_assertion wasGeneratedBy ECO_0000203 NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP63511.RAvL9i_AK_LVwdQiOn_avaOIddGZygzYaXLXJpjD0FbGg130_provenance.