Matches in Nanopublications for { ?s ?p "[Because ASXL1 lesions have been increasingly identified in myeloid neoplasms, we examined the relationships of ASXL1 mutation or deletion to both clinical phenotype and associated molecular features in 166 patients with myeloproliferative neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP255032.RAJK4cOfcT9Vo3Fp9cZcPUa66J_h5WxcdHD-4b-bX_E00130_assertion description "[Because ASXL1 lesions have been increasingly identified in myeloid neoplasms, we examined the relationships of ASXL1 mutation or deletion to both clinical phenotype and associated molecular features in 166 patients with myeloproliferative neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255032.RAJK4cOfcT9Vo3Fp9cZcPUa66J_h5WxcdHD-4b-bX_E00130_provenance.
- assertion description "[Because ASXL1 lesions have been increasingly identified in myeloid neoplasms, we examined the relationships of ASXL1 mutation or deletion to both clinical phenotype and associated molecular features in 166 patients with myeloproliferative neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP978552.RA3SUp4R3OHn8Nr0NmvtKveVVHd_c7xEuyWQc_pZJseSA130_assertion description "[Because ASXL1 lesions have been increasingly identified in myeloid neoplasms, we examined the relationships of ASXL1 mutation or deletion to both clinical phenotype and associated molecular features in 166 patients with myeloproliferative neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978552.RA3SUp4R3OHn8Nr0NmvtKveVVHd_c7xEuyWQc_pZJseSA130_provenance.