Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_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." NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_assertion evidence source_evidence_literature NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_assertion SIO_000772 3283935 NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_assertion wasDerivedFrom befree-20140225 NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_assertion wasGeneratedBy ECO_0000203 NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869346.RAWh3zG89eKmN-IH4y39TQMTvsmJzQzAC9TT0njINrAJE130_provenance.