Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion> ?p ?o ?g. }
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- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion type Assertion NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_head.
- 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.
- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion evidence source_evidence_literature NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_provenance.
- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion SIO_000772 23824601 NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_provenance.
- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion wasDerivedFrom befree-2016 NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_provenance.
- NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_assertion wasGeneratedBy ECO_0000203 NP1091107.RAyP6PyI2sNhiZGdolHP4jV1IgP6qduVhkK1jLVLqpGoA130_provenance.