Matches in Nanopublications for { ?s ?p "[Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP615044.RAS-V_GtW1eG_3ewSVjUA144_RS6Gw_1W-lYGqlzeOkso130_assertion description "[Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615044.RAS-V_GtW1eG_3ewSVjUA144_RS6Gw_1W-lYGqlzeOkso130_provenance.
- NP708797.RATM0URYblljH9AT86hs8bZbFA2QCkTNB--ju8EDxgBlY130_assertion description "[Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708797.RATM0URYblljH9AT86hs8bZbFA2QCkTNB--ju8EDxgBlY130_provenance.
- NP660578.RA-jbuHUvSGa4yZ34YZCwiwe3VjpHeX_TT4HzbiGtW-to130_assertion description "[Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660578.RA-jbuHUvSGa4yZ34YZCwiwe3VjpHeX_TT4HzbiGtW-to130_provenance.