Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP641571.RAiT3wD7SKsqFjxwOZfVxNdQ7YaIDUK1JYl3CxIn_UBic#assertion> ?p ?o ?g. }
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- assertion description "[Congenital leptin deficiency, a rare genetic disorder due to a homozygous mutation in the leptin gene (LEP), is accompanied by extreme obesity and hyperphagia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 23824601 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.