Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_assertion description "[Low ERG and BAALC expression (E/B(low)) and NOTCH1/FBXW7 (N/F) mutations have been proposed as powerful prognostic markers in large cohorts of adult T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_assertion evidence source_evidence_literature NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_assertion SIO_000772 21835957 NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_assertion wasDerivedFrom befree-20140225 NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_assertion wasGeneratedBy ECO_0000203 NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171222.RA1Swar6_daqaQSjy-OA28TovHJ4t3yZWn4nt2WynDWZ4130_provenance.