Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_assertion description "[SRSF2 and U2AF1 along with TET2 (48%) and ASXL1 (38%) are frequently affected by somatic mutations in chronic myelomonocytic leukemia, quite distinctly from the profile seen in juvenile myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_assertion evidence source_evidence_literature NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_assertion SIO_000772 22773603 NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_assertion wasDerivedFrom befree-20150227 NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_assertion wasGeneratedBy ECO_0000203 NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1018524.RAHCxPtWqPf4A2RGsVMQNMmeDJYn2U_VTiL44YNku0zhw130_provenance.