Matches in Nanopublications for { ?s ?p "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP396186.RAU_fNlrpIQLDk8DxnRcHgELHFfI2e9kjflDN7siMlcO8130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396186.RAU_fNlrpIQLDk8DxnRcHgELHFfI2e9kjflDN7siMlcO8130_provenance.
- NP453930.RA4PvLuIij4i5akxB7u1tT_eUwvEA0MS9_D6Ndilgn-Pg130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453930.RA4PvLuIij4i5akxB7u1tT_eUwvEA0MS9_D6Ndilgn-Pg130_provenance.
- NP371418.RAXh5MYj3aV1GjxhL8N8AuThXHfCggqBEKI5Apv8-WBKE130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371418.RAXh5MYj3aV1GjxhL8N8AuThXHfCggqBEKI5Apv8-WBKE130_provenance.
- NP371423.RAempXJ2UFaNC7G50M2cdzYrFNWkYmlQ4Q0sJ1I0An8aI130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371423.RAempXJ2UFaNC7G50M2cdzYrFNWkYmlQ4Q0sJ1I0An8aI130_provenance.
- NP638419.RAwCOS7j057Hv97QpgcddCvSNZrWdprbPrjkCA4npUaQ8130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638419.RAwCOS7j057Hv97QpgcddCvSNZrWdprbPrjkCA4npUaQ8130_provenance.
- NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873361.RActQS1IgcMyiUZRTTLzP7C9Kj9F_NHTNuWKLyN9kl3zw130_provenance.
- NP469792.RANyTLzGOOkNEmD5zOpOd8vStBtDWSuO6IPbG1ZxUaeuQ130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469792.RANyTLzGOOkNEmD5zOpOd8vStBtDWSuO6IPbG1ZxUaeuQ130_provenance.
- NP465657.RAIgSitbMy9casabPCJw1ovnD0FcXoWUybanuIyklN8kU130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465657.RAIgSitbMy9casabPCJw1ovnD0FcXoWUybanuIyklN8kU130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP1088244.RA4HIni8Y_Xtd8XWX2X3M1quz1nLwozRR1Sap68_0gdEw130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088244.RA4HIni8Y_Xtd8XWX2X3M1quz1nLwozRR1Sap68_0gdEw130_provenance.