Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion type Assertion NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_head.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion wasGeneratedBy ECO_0000203 NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_provenance.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion wasDerivedFrom befree-2016 NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_provenance.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion SIO_000772 12850377 NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_provenance.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion evidence source_evidence_literature NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_provenance.
- NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_assertion description "[The cryptic translocation t(12;21)(p13;q22), which leads to the TEL-AML1 fusion gene, is the most common abnormality in childhood B-cell ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401201.RAAsOH7Yk_xkj8636H86y20NBTInuw59zySVsK7tHZ2o0130_provenance.