Matches in Nanopublications for { ?s ?p "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 8 of
8
with 100 items per page.
- NP877610.RAlyHt9wKJU2HA6K-FHT269eKQtFPShbwKASQ7e493YWg130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877610.RAlyHt9wKJU2HA6K-FHT269eKQtFPShbwKASQ7e493YWg130_provenance.
- NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220578.RA8SVMt2iH4mNnvqee_iyUqoE5A74xLKcdd7DqVsPc7JA130_provenance.
- assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP444800.RAf7L0dCjXbPQ_3buhiYDOnzTDCy967jzhO0uB3JwsUzw130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444800.RAf7L0dCjXbPQ_3buhiYDOnzTDCy967jzhO0uB3JwsUzw130_provenance.
- NP444743.RABJhHt5QfvA0n4kVs8UJe_6jC627_NwhDF-dFRtPkGzo130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444743.RABJhHt5QfvA0n4kVs8UJe_6jC627_NwhDF-dFRtPkGzo130_provenance.
- NP1307268.RAgAgPhK2VNk2iu2bZ9efhX63CDzcRDkTBqp0GMAuLMnM130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307268.RAgAgPhK2VNk2iu2bZ9efhX63CDzcRDkTBqp0GMAuLMnM130_provenance.
- NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_assertion description "[Whereas individuals heterozygous for most alpha-chain mutations possess approximately 25% abnormal hemoglobin, heterozygotes for the alpha-chain variant Hb G Philadelphia synthesize either 33% or 50% Hb G. Both variable gene dosage and interaction with alpha-thalassemia have been proposed to explain this observation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307269.RAnbrqfB3HxjS6lPDndA6YS4mmKAxL4nHY0S7GFUXKL_s130_provenance.