Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion type Assertion NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_head.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion evidence source_evidence_literature NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion SIO_000772 7156322 NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion wasDerivedFrom befree-20150227 NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion wasGeneratedBy ECO_0000203 NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.