Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_assertion description "[We conclude that FCGR3B deletion juxtaposes the 5'-regulatory sequences of FCGR2C with the coding sequence of FCGR2B, creating a chimeric gene that results in an ectopic accumulation of Fc?RIIb on NK cells and provides an explanation for SLE risk associated with reduced FCGR3B gene copy number.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_assertion evidence source_evidence_literature NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_assertion SIO_000772 23261299 NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_assertion wasDerivedFrom befree-20140225 NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_assertion wasGeneratedBy ECO_0000203 NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312671.RApiJQWo9ux90VwRkn6dHnoY3lkG4t8Pi4zG_J9hLs_oo130_provenance.