Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion> ?p ?o ?g. }
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- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion type Assertion NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_head.
- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion description "[A mutant form of apolipoprotein E that is defective in binding to low density lipoprotein receptors is associated with familial type III hyperlipoproteinemia, a genetic disorder characterized by elevated plasma cholesterol levels and accelerated coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion evidence source_evidence_literature NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion SIO_000772 3283935 NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion wasDerivedFrom befree-2016 NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_assertion wasGeneratedBy ECO_0000203 NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.