Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_assertion description "[The preliminary results obtained in this study revealed an association of the MTHFR and APOE gene polymorphism with cerebrovascular disease, suggesting a significant risk for stroke in subjects who are homozygous for the T allele and for carotid stenosis in subjects having APOEepsilon3epsilon4 genotype. Additional studies in larger patient groups are needed to confirm these observations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_assertion evidence source_evidence_literature NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_assertion SIO_000772 11388660 NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_assertion wasDerivedFrom gad-20130706 NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_assertion wasGeneratedBy ECO_0000203 NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52933.RAQz3FnI93LMVEvHjKHhMCNqTZO7_WsHLo93w4IF-FPOo130_provenance.