Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion type Assertion NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_head.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_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." NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_provenance.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion evidence source_evidence_literature NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_provenance.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion SIO_000772 12850377 NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_provenance.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion wasDerivedFrom befree-2016 NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_provenance.
- NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_assertion wasGeneratedBy ECO_0000203 NP401197.RAjSdCsGIzJfUNGoPPuF7aitxxXYnb0MqCtdT2QuMah7M130_provenance.