Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion> ?p ?o ?g. }
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- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion type Assertion NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_head.
- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion description "[Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive syndrome characterized by extreme paucity of adipose tissue since birth, acanthosis nigricans, severe insulin resistance, marked hypertriglyceridemia, and early-onset diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_provenance.
- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion evidence source_evidence_literature NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_provenance.
- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion SIO_000772 14602785 NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_provenance.
- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion wasDerivedFrom befree-20140225 NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_provenance.
- NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_assertion wasGeneratedBy ECO_0000203 NP671869.RAe-E_hFy1VLqH5SNZ5AQj49Sa2mdtxsQ4cqJtlIFdJCw130_provenance.