Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_assertion description "[we observe significant association with risk for AD and polymorphisms in ACE, CHRNB2, TF, and an as yet uncharacterized locus on chromosome 7p15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_assertion evidence source_evidence_literature NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_assertion SIO_000772 18830724 NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_assertion wasDerivedFrom gad-20130706 NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_assertion wasGeneratedBy ECO_0000203 NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.
- gad-20130706 importedOn "2013-07-06" NP69227.RAGJYHjExnu8BrG606q5D1WkY4scVLJ297op5V8Dhti44130_provenance.