Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion> ?p ?o ?g. }
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- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion type Assertion NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_head.
- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_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." NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_provenance.
- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion evidence source_evidence_literature NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_provenance.
- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion SIO_000772 15973457 NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_provenance.
- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion wasDerivedFrom befree-20140225 NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_provenance.
- NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_assertion wasGeneratedBy ECO_0000203 NP467274.RAPmi_3LmwgPVF_1ZSuYRou1eelgEk9ApZc_OVifl5a7Q130_provenance.