Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion type Assertion NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_head.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion description "[Autosomal recessive hypercholesterolaemia (ARH), characterized clinically by severe inherited hypercholesterolaemia, is caused by recessive null mutations in LDLRAP1 (formerly ARH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion evidence source_evidence_literature NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion SIO_000772 17761685 NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion wasDerivedFrom befree-20140225 NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion wasGeneratedBy ECO_0000203 NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.