Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion> ?p ?o ?g. }
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- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion type Assertion NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_head.
- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion wasGeneratedBy ECO_0000203 NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_provenance.
- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion wasDerivedFrom befree-20140225 NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_provenance.
- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion SIO_000772 12850377 NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_provenance.
- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_assertion evidence source_evidence_literature NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_provenance.
- NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_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." NP654394.RAAH9lyF_ULE9KACqqZr9Pc4eRwytzW4VpUZmUVx29jCM130_provenance.