Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_assertion description "[These data suggest that NOTCH1/FBXW7 mutations are present in T-ALL patients from Southern India and may be useful biomarkers to predict prognosis in T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_assertion evidence source_evidence_literature NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_assertion SIO_000772 25493453 NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_assertion wasDerivedFrom befree-20150227 NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_assertion wasGeneratedBy ECO_0000203 NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP595696.RAMxVVOFW2uP61Oevsz0RFM1LgQeTPL5utiQ9CLWH1QE4130_provenance.