Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_assertion description "[Among 18 BCR-ABL+ leukemias presenting acquired trisomy of chromosome 21, we report a high frequency (33%) of recurrent point mutations (4 in myeloid blast crisis [BC] CML and one in chronic phase CML) within the DNA-binding region of RUNX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_assertion evidence source_evidence_literature NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_assertion SIO_000772 18202228 NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_assertion wasDerivedFrom befree-2016 NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_assertion wasGeneratedBy ECO_0000203 NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.
- befree-2016 importedOn "2016-02-19" NP650506.RAMkVyPbcKE3Vm2j-R7fF2OfeWvWPV9caQ-w937BuoZL8130_provenance.