Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_assertion description "[CHRFAM7A transcript levels in CD4+ T-lymphocytes were compared between ADNFLE patients harbouring the c.851C>T mutation of the CHRNA4 gene and control healthy individuals in order to determine whether there is any correlation between CHRFAM7A expression in CD4+ T-lymphocytes and the severity of epileptic symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_assertion evidence source_evidence_literature NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_assertion SIO_000772 23553139 NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_assertion wasDerivedFrom befree-20140225 NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_assertion wasGeneratedBy ECO_0000203 NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP520583.RAuQ0GLmYh0bmdrvj7tS2K-LjaBpCTFlHyPMrEK7IA_h4130_provenance.