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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- 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." provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_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." NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.