Matches in Nanopublications for { ?s ?p "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP289151.RAR1UCCTQladSJ2wsE5zATrIa7m42umy9Aq4XZoC15J1o130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289151.RAR1UCCTQladSJ2wsE5zATrIa7m42umy9Aq4XZoC15J1o130_provenance.
- NP289214.RAR_HYClAsj0jeeVsU0U9Qotk_l4QPCD3RHnhTVky9xVk130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289214.RAR_HYClAsj0jeeVsU0U9Qotk_l4QPCD3RHnhTVky9xVk130_provenance.
- NP387109.RAZzoyUQheahr9AffamFJJUlxaRcLrTiMuMcJHxOIgHos130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387109.RAZzoyUQheahr9AffamFJJUlxaRcLrTiMuMcJHxOIgHos130_provenance.
- NP1186376.RA3CbmvBlwN0PqerqHAZPMdpumTnwZ3zTOa5Rh2R2ZDQ0130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186376.RA3CbmvBlwN0PqerqHAZPMdpumTnwZ3zTOa5Rh2R2ZDQ0130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP1186373.RAYtzb35olfXjNkRhFFGeOqPfWF_wmdHNHQMoq-Vo_W2Q130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186373.RAYtzb35olfXjNkRhFFGeOqPfWF_wmdHNHQMoq-Vo_W2Q130_provenance.
- NP1186374.RAJTN0m0JwliU75BTBe9xxdB63b_ZMCHGOx_EwTW7ONKU130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186374.RAJTN0m0JwliU75BTBe9xxdB63b_ZMCHGOx_EwTW7ONKU130_provenance.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.
- NP1186377.RApBomOPoF-x5DvUIqVik53aQC7l69dd4r4IHwfSyyEAA130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186377.RApBomOPoF-x5DvUIqVik53aQC7l69dd4r4IHwfSyyEAA130_provenance.