Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_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." NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_assertion evidence source_evidence_literature NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_assertion SIO_000772 23553139 NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_assertion wasDerivedFrom befree-20140225 NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_assertion wasGeneratedBy ECO_0000203 NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP334736.RARMb_3X6MGD7UdRK_ZMeqeg43Q2dPxWWTeW3E4p17VDk130_provenance.