Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion> ?p ?o ?g. }
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- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion type Assertion NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_head.
- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion wasGeneratedBy ECO_0000203 NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance.
- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion wasDerivedFrom befree-2016 NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance.
- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion SIO_000772 11714841 NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance.
- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion evidence source_evidence_literature NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance.
- NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion description "[The identification of mutations in ABCA1 in patients with Tangier disease and familial HDL deficiency demonstrated that inadequate transport of phospholipid and cholesterol to the extracellular space results in the hypercatabolism of lipid-poor nascent HDL particles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance.