Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP533977.RAaZenVZNDAOXQ21lqYUx6bivR1G16k_1y472C7QX_0JI130_provenance.