Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_assertion description "[In humans, mutations in leptin, leptin receptor, proopiomelanocortin (POMC), melanocortin-4 receptor (MC4R) and prohormone convertase 1 (PC1) have been described in patients with severe obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_assertion evidence source_evidence_literature NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_assertion SIO_000772 11924926 NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_assertion wasDerivedFrom befree-20140225 NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_assertion wasGeneratedBy ECO_0000203 NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239486.RA0kfW_yz48KeZ5q12U4WEEoYTXgeKQZP-g3ZygdZPybY130_provenance.