Matches in Nanopublications for { ?s ?p "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP351761.RAU9QkG-gmZSIFwhfoUs24miwjuCGWLfdHhJ2FeW-9QDw130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351761.RAU9QkG-gmZSIFwhfoUs24miwjuCGWLfdHhJ2FeW-9QDw130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792223.RAQIExJLIbUM0p3RxebxRDWR76u5z1Xqro5gn4O1WtPiI130_provenance.
- NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792228.RAlEQaGQ33P_5IF2bQXsB7Nl0QfzYmPr7q5MgJcjtHp4Q130_provenance.