@prefix this: . @prefix sub: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-gda: . @prefix dgn-void: . sub:head { this: np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:publicationInfo; a np:Nanopublication . } sub:assertion { dgn-gda:DGN43ee4572813daff4b0c144e3852c22d5 sio:SIO_000628 miriam-gene:5443, lld:C0027627; a sio:SIO_001122 . } sub:provenance { sub:assertion dcterms:description "[We identified seven independent loci (P < 5.0 � 10??) near FTO (P = 3.72 � 10?��), TMEM18 (P = 3.24 � 10?�?), MC4R (P = 4.41 � 10?�?), TNNI3K (P = 4.32 � 10?��), SEC16B (P = 6.24 � 10??), GNPDA2 (P = 1.11 � 10??) and POMC (P = 4.94 � 10??) as well as a potential secondary signal at the POMC locus (rs2118404, P = 2.4 � 10?? after conditioning on the established single-nucleotide polymorphism at this locus) in adolescents and young adults.]. 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:23669352; prov:wasDerivedFrom dgn-void:BEFREE; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:BEFREE pav:importedOn "2017-02-19"^^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 . } sub:publicationInfo { this: dcterms:created "2017-10-17T13:15:31+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 "v5.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v5.0.0" . }