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- source_evidence_literature type ECO_0000212 NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_assertion description "[We conclude that there are rare patients with CML who either present in blast crisis with coexistence of t(9;22) and t(8;21) with or without +8, or progress to blast crisis with acquiring RUNX1-RUNX1T1 in the BCR-ABL1 clone which may or may not be therapy related and represent a later event in a multistep pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_assertion evidence source_evidence_literature NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_assertion SIO_000772 21504717 NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_assertion wasDerivedFrom befree-2016 NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_assertion wasGeneratedBy ECO_0000203 NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.
- befree-2016 importedOn "2016-02-19" NP888306.RAes6LWdG9GkohpX07YxcRDVHxaGKbLdgUPb2xVVaMkpY130_provenance.