Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion> ?p ?o ?g. }
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- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion type Assertion NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_head.
- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion description "[We report a rare cryptic ins(12;9)(p13;q34q34), a chromosomal abnormality involving the ABL1 (9q34) and the ETV6 (alias TEL; 12p13) genes, detectable only by fluorescence in situ hybridization (FISH), in a patient with Philadelphia-negative chronic myeloid leukemia (CML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_provenance.
- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion evidence source_evidence_literature NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_provenance.
- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion SIO_000772 19480935 NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_provenance.
- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion wasDerivedFrom befree-2016 NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_provenance.
- NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_assertion wasGeneratedBy ECO_0000203 NP741943.RAdEgh3HAb4Fx482JEo3n6devFcxN1rDoBmNKAiRX1GgE130_provenance.