Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- befree-2016 importedOn "2016-02-19" NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_assertion wasGeneratedBy ECO_0000203 NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_assertion wasDerivedFrom befree-2016 NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_assertion SIO_000772 12764379 NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_assertion evidence source_evidence_literature NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.
- NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_assertion description "[Our results show that most BCR/ABL+ patients (83%, including 88% of all CML, 61% of ALL and one of two AML) displayed typical iFISH patterns of either Major (M) BCR/ABL (87% of CML, 13% of ALL and one of the two AML) or minor (m) BCR/ABL gene rearrangements (1% of all CML and 48% of ALL cases) with the two probes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395423.RAxkvlCPOwtMX-Zgenhv2D-6BlI-iQ8-Eo1Ndxrsp2dms130_provenance.