Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion> ?p ?o ?g. }
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- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion type Assertion NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_head.
- 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.
- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion evidence source_evidence_literature NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion SIO_000772 23824601 NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion wasDerivedFrom befree-20150227 NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_assertion wasGeneratedBy ECO_0000203 NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.