Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion evidence source_evidence_literature NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion SIO_000772 23415222 NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion wasDerivedFrom befree-20140225 NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion wasGeneratedBy ECO_0000203 NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.