Matches in Nanopublications for { ?s ?p "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.
- assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.
- NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_provenance.