Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_assertion description "[We conclude that FLT3 mutation is rare in T-ALL, and its presence supports T/myeloid lineage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_assertion evidence source_evidence_literature NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_assertion SIO_000772 22261446 NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_assertion wasDerivedFrom befree-20140225 NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_assertion wasGeneratedBy ECO_0000203 NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP187309.RA88hjZUA9ngHQ1veIOnlu714R6qP3m2umIZsBPtcf1Zw130_provenance.