Matches in Nanopublications for { ?s ?p "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP581548.RAY95QbzeR20LD59mJ0oiF_2tIXYC6m36dGOC72lQyHeY130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581548.RAY95QbzeR20LD59mJ0oiF_2tIXYC6m36dGOC72lQyHeY130_provenance.
- NP548938.RAiwGG1A7ubfmDVSWIEX6dVH8unTXEZJNmPDFI_TdQmZ4130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548938.RAiwGG1A7ubfmDVSWIEX6dVH8unTXEZJNmPDFI_TdQmZ4130_provenance.
- NP389627.RAD5_QuyKhZLkuEIMKckah3WNihTMekTsg1ZlG9y3T96M130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389627.RAD5_QuyKhZLkuEIMKckah3WNihTMekTsg1ZlG9y3T96M130_provenance.
- NP854340.RA8sizQmx7Abf5WOAkpALPh1GuMTPWr72_QxO3RTglbq0130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854340.RA8sizQmx7Abf5WOAkpALPh1GuMTPWr72_QxO3RTglbq0130_provenance.
- NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389380.RA9KaHw5_ogjfrx-YckMhcioJojxggdeeoWfIbUIM1pCU130_provenance.
- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_provenance.
- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_provenance.
- NP503979.RAH_YdAuJqDjj1dKlzkgYv6RZFEU7dxuNUHr3cYYMChwk130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503979.RAH_YdAuJqDjj1dKlzkgYv6RZFEU7dxuNUHr3cYYMChwk130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.