Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_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." NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_assertion evidence source_evidence_literature NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_assertion SIO_000772 11924926 NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_assertion wasDerivedFrom befree-20140225 NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_assertion wasGeneratedBy ECO_0000203 NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP225746.RAFIIbqJ-Pouns0p1hIKWIjne6AH0Z9VJMSVvhviJYWD8130_provenance.