Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion> ?p ?o ?g. }
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- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion type Assertion NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_head.
- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion wasGeneratedBy ECO_0000203 NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_provenance.
- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion wasDerivedFrom befree-20150227 NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_provenance.
- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion SIO_000772 12453919 NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_provenance.
- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion evidence source_evidence_literature NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_provenance.
- NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_assertion description "[Autosomal dominant familial partial lipodystrophy (FPLD) due to mutant LMNA encoding nuclear lamin A/C is characterized by adipose tissue repartitioning together with multiple metabolic disturbances, including insulin resistance and dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537622.RAuWD512L71PT0EdYTuprBKty7H9RlFNjson_92TywfVM130_provenance.