Matches in Nanopublications for { ?s ?p "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP239729.RALB0iIKQd5FvXuD3u2vkZtqr1Y0GRNaU8M6PW50qWV4Y130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239729.RALB0iIKQd5FvXuD3u2vkZtqr1Y0GRNaU8M6PW50qWV4Y130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP600946.RAI1a23DA3IIlRYO2WVrtl-634KvexVXXgafrlo_ZFdMs130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600946.RAI1a23DA3IIlRYO2WVrtl-634KvexVXXgafrlo_ZFdMs130_provenance.