Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_assertion wasGeneratedBy ECO_0000203 NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_assertion wasDerivedFrom befree-2016 NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_assertion SIO_000772 25670367 NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_assertion evidence source_evidence_literature NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.
- NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_assertion description "[Previous studies have shown that patients with autosomal recessive hypercholesterolemia (ARH) resulting from mutations in LDLRAP1 gene have a less severe cardiovascular involvement than familial hypercholesterolemia homozygotes, lower levels of low-density lipoprotein cholesterol (LDL-C), and higher levels of high-density lipoprotein cholesterol (HDL-C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1262646.RAH-PQiXg8jNBilTQvK9lKGXUQXtbS5QHJrVxcKreDrDs130_provenance.