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- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion type Assertion NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_head.
- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion wasGeneratedBy ECO_0000203 NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_provenance.
- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion wasDerivedFrom befree-2016 NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_provenance.
- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion SIO_000772 16015425 NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_provenance.
- NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_assertion evidence source_evidence_literature NP503980.RAVy8KhiXXwxgXLUfI98K-yu_U2FrJenEHeVcwJhbERfc130_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.