Matches in Nanopublications for { ?s ?p "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220393.RAPkdY3NZPxjT_LVa0Gz9BxuFm8BhNMZ6GTTYYX8wCOAs130_provenance.
- NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465069.RACRA9s7-mGsZcA54Iai_OeelDzFj4-xL9zFP3o8cdzwc130_provenance.
- assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378106.RAMPqZTjytZF4ADDejPuCTpSDX-vmTrKsjIbXK4WVkjZ8130_provenance.
- NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398536.RAzZV_xkdGU74ZYHXdqzxbLZ0jBKxSX5OjrdZs7F6h1Ns130_provenance.
- NP1398539.RA9y_7ZIcGNBYKEqigMUAyDsmkvMxSJQpgQ300rBZ8S4A130_assertion description "[Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare proliferative disorder of erythroid progenitor cells, characterized by elevated erythrocyte mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to erythropoietin (EPO), and autosomal dominant inheritance or sporadic occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398539.RA9y_7ZIcGNBYKEqigMUAyDsmkvMxSJQpgQ300rBZ8S4A130_provenance.