Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion> ?p ?o ?g. }
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- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion type Assertion NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_head.
- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion wasGeneratedBy ECO_0000203 NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_provenance.
- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion wasDerivedFrom gad-20150221 NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_provenance.
- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion SIO_000772 17650440 NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_provenance.
- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion evidence source_evidence_literature NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_provenance.
- NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_assertion description "[The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108061.RAYYwXVX730pdD3_ypHozeoPwspgCeFeX-tNLUkasqCYk130_provenance.