Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_assertion description "[Cytogenetic and flow cytometry evaluation of Richter syndrome reveals MYC, CDKN2A, IGH alterations with loss of CD52, CD62L and increase of CD71 antigen expression as the most frequent recurrent abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_assertion evidence source_evidence_literature NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_assertion SIO_000772 25511139 NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_assertion wasDerivedFrom befree-20150227 NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_assertion wasGeneratedBy ECO_0000203 NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP581873.RAdhXH25HqofnMUOs9yl45ZLFH8YUdfoDkXeA_YfrAvfo130_provenance.