Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion> ?p ?o ?g. }
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- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion type Assertion NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_head.
- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion description "[The t(6;9)(p23;q34) is a recurrent chromosomal abnormality observed in 1% of acute myelogenous leukemia (AML), which generates a fusion transcript between DEK and CAN/NUP214 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_provenance.
- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion evidence source_evidence_literature NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_provenance.
- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion SIO_000772 15973457 NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_provenance.
- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion wasDerivedFrom befree-20150227 NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_provenance.
- NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_assertion wasGeneratedBy ECO_0000203 NP785861.RAODSGpYk1T1xQdgci7OJsanVUcb_K3_9K8KF_RbKQSqc130_provenance.