Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP199660.RAZYtUHzVfv1K6VVUYgJqPscbSatVRILd5OvjMkOTrRP4130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199660.RAZYtUHzVfv1K6VVUYgJqPscbSatVRILd5OvjMkOTrRP4130_provenance.
• NP221911.RAZYWv6xKknQcaFuloY2bGfIHu24SmfGMoUmK2NCuzoLI130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221911.RAZYWv6xKknQcaFuloY2bGfIHu24SmfGMoUmK2NCuzoLI130_provenance.
• NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.
• NP739470.RAiF96KPEHHmhcTzz8vUJZS0k1f40_kTH6D_lJDMaHwIw130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739470.RAiF96KPEHHmhcTzz8vUJZS0k1f40_kTH6D_lJDMaHwIw130_provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
• NP547266.RAn4mricCGx7fENFoNUHg8ViZ8g843OBSW30Ehn9ju7eI130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547266.RAn4mricCGx7fENFoNUHg8ViZ8g843OBSW30Ehn9ju7eI130_provenance.
• NP547275.RAJWn39xoJjrQ2QbwSCO6fFPwBUK-UsFcApCjY6wR04ps130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547275.RAJWn39xoJjrQ2QbwSCO6fFPwBUK-UsFcApCjY6wR04ps130_provenance.
• NP547267.RA3OW2C0NWztbY4VRpuxVJce-IhJVzx57zD2iMrj3Nfdw130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547267.RA3OW2C0NWztbY4VRpuxVJce-IhJVzx57zD2iMrj3Nfdw130_provenance.
• NP547268.RA3tqDYbWe3BCDlrpZmd4Ys85Gr8z-iV3MMGMDGON5jJY130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547268.RA3tqDYbWe3BCDlrpZmd4Ys85Gr8z-iV3MMGMDGON5jJY130_provenance.
• NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
• NP547270.RAyrAI2ENoM4j7OcUsCLHLZGTR2FF7vdz6UcjZDFhUDdU130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547270.RAyrAI2ENoM4j7OcUsCLHLZGTR2FF7vdz6UcjZDFhUDdU130_provenance.
• NP547271.RA2wY3i8021NG2EEKsDoBnRa1vyEyYW6-upZtg8QcmGgI130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547271.RA2wY3i8021NG2EEKsDoBnRa1vyEyYW6-upZtg8QcmGgI130_provenance.
• NP547273.RA1ZbuXTcXqipiwwOvdyCF1x-ecPvXSdVO9xsjMGCnzAM130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547273.RA1ZbuXTcXqipiwwOvdyCF1x-ecPvXSdVO9xsjMGCnzAM130_provenance.
• NP547274.RAxubxrB6FgwZSAZzbU929TY2deraFbz-YX8OKA_wayqw130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547274.RAxubxrB6FgwZSAZzbU929TY2deraFbz-YX8OKA_wayqw130_provenance.