Matches in Nanopublications for { ?s ?p "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion description "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion description "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.