Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_assertion description "[Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_assertion evidence source_evidence_literature NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_assertion SIO_000772 16757412 NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_assertion wasDerivedFrom befree-2016 NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_assertion wasGeneratedBy ECO_0000203 NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP553374.RAHTxT_D9kHfD9K9LR6Oe5y5TOs446EgEloYNzvxLrt2Y130_provenance.