Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_assertion description "[In addition to congenital leptin deficiency, conditions that may be associated with decreased leptin levels include hypothalamic amenorrhea, anorexia nervosa, and congenital or acquired lipodystrophy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_assertion evidence source_evidence_literature NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_assertion SIO_000772 22665330 NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_assertion wasDerivedFrom befree-20150227 NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_assertion wasGeneratedBy ECO_0000203 NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP534691.RAf5VGpST5-468OErdkS0nEvzsb6MSMjOpo2zV4D3hRWE130_provenance.