Matches in Nanopublications for { ?s ?p "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion description "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion description "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.