Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_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." NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- 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.
- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_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." NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_provenance.