Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1301152.RA6Og0QK0TjlODySg38v7df26v4GoGVIbrl72sGmCXS2Q130_provenance.