Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_assertion description "[In this report, we have identified an identical point mutation in two human B-cell lymphomas (follicular (FL) and mediastinal) that changes serine (Ser)525 (TCA) to proline (Pro) (CCA) within the REL transactivation domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_assertion evidence source_evidence_literature NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_assertion SIO_000772 17072339 NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_assertion wasDerivedFrom befree-20140225 NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_assertion wasGeneratedBy ECO_0000203 NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP469058.RA_yHUZhBUNLXcYO69_7frZunFlIL5onh56k3kHr1aUBM130_provenance.