Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion type Assertion NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_head.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion description "[Levels of lipoprotein(a) are primarily determined by variation in the LPA gene coding for the apolipoprotein(a) moiety of lipoprotein(a), and genetic epidemiologic studies have documented association of LPA copy number variants, influencing levels of lipoprotein(a), with risk of IHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_provenance.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion evidence source_evidence_literature NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_provenance.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion SIO_000772 20106478 NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_provenance.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion wasDerivedFrom befree-2016 NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_provenance.
- NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_assertion wasGeneratedBy ECO_0000203 NP789864.RAivm1r_XQHT3VyUfA55bTi66gNNm9yOpNhqLp1mIsDoY130_provenance.