Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion> ?p ?o ?g. }
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- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion type Assertion NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_head.
- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_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." NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_provenance.
- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion evidence source_evidence_literature NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_provenance.
- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion SIO_000772 15973457 NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_provenance.
- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion wasDerivedFrom befree-20140225 NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_provenance.
- NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_assertion wasGeneratedBy ECO_0000203 NP349862.RAEkFzL4V2_LmCZXm8OQTYOo2aHfiyRttMzM97h3xso24130_provenance.