@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_head { this: np:hasAssertion dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_assertion; np:hasProvenance dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_provenance; np:hasPublicationInfo dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_publicationInfo; a np:Nanopublication . dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_assertion a np:Assertion . dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_provenance a np:Provenance . dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_publicationInfo a np:PublicationInfo . } dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_assertion { miriam-gene:3953 a ncit:C16612 . lld:C0028754 a ncit:C7057 . dgn-gda:DGN9947bc48d583dd7795659805ee0065c6 sio:SIO_000628 miriam-gene:3953, lld:C0028754; a sio:SIO_001121 . } dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_provenance { dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_assertion dcterms:description "[In obese humans, ob/ob like mutations in leptin are rare but confirm a role for leptin (Montague et al., 1997), and db/db like mutations in the leptin receptor have not been found (Considine et al., 1996a); however, the increased understanding of the molecular basis for obesity has generated tremendous interest among scientists and patients alike.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:9516053; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1391317.RAe5T0oOL-Mx8Ml6qpZrR1s8-FggODAOUtiIcjb5vB93s130_publicationInfo { this: dcterms:created "2016-05-13T12:52:17+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }