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- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion type Assertion NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_head.
- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion wasGeneratedBy ECO_0000203 NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_provenance.
- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion wasDerivedFrom befree-20150227 NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_provenance.
- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion SIO_000772 16015425 NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_provenance.
- NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_assertion evidence source_evidence_literature NP389949.RAF4mESZgp3kX4O-0r28QKl3JeELFe1fNau9qMud0FrEE130_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.