Matches in Nanopublications for { ?s ?p "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP82720.RAYldTmrtlqk20y_1sdF51MLgcnKJerSC_31oqBmAFzVw130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82720.RAYldTmrtlqk20y_1sdF51MLgcnKJerSC_31oqBmAFzVw130_provenance.
- NP79928.RA5nlvfcaJ0PcB6tmHRUqdWw9aKO9oX53H2ogEZh82DPA130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79928.RA5nlvfcaJ0PcB6tmHRUqdWw9aKO9oX53H2ogEZh82DPA130_provenance.
- NP97231.RA2QTctdFXCu8dPudZxc0lzqqxkDCUkQRpEYX88xpvLy0130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97231.RA2QTctdFXCu8dPudZxc0lzqqxkDCUkQRpEYX88xpvLy0130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP58434.RAuDhceRQvGHncBt4CSaBFiuplOuTKeQKDrU8KubPhe4A130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58434.RAuDhceRQvGHncBt4CSaBFiuplOuTKeQKDrU8KubPhe4A130_provenance.
- NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66083.RAoEp4FyzyoO9lnp2ZwEOEFNaoWiloIQCLxNZKjzi1Ka0130_provenance.
- NP97230.RAqYUllsLkddS732quKAHm9e8LXDI4umLWucdsIzL5ILs130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97230.RAqYUllsLkddS732quKAHm9e8LXDI4umLWucdsIzL5ILs130_provenance.
- NP97232.RAnuGzLRYhct7-CoZQiLTuEeswd-3reRRq6BgzUNqSRSo130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97232.RAnuGzLRYhct7-CoZQiLTuEeswd-3reRRq6BgzUNqSRSo130_provenance.