@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:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_head { this: np:hasAssertion dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_assertion; np:hasProvenance dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_provenance; np:hasPublicationInfo dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_publicationInfo; a np:Nanopublication . dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_assertion a np:Assertion . dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_provenance a np:Provenance . dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_publicationInfo a np:PublicationInfo . } dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_assertion { miriam-gene:4864 a ncit:C16612 . lld:C0028754 a ncit:C7057 . dgn-gda:DGN075d436955cadbdabf04027f1114c425 sio:SIO_000628 miriam-gene:4864, lld:C0028754; a sio:SIO_001122 . } dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_provenance { dgn-np:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_assertion dcterms:description "[There is evidence that the obesity phenotype in the Caucasian populations is associated with variations in several genes, including neuronal growth regulator 1 (NEGR1), SEC16 homolog B (SCE16B), transmembrane protein 18 (TMEM18), ets variant 5 (ETV5), glucosamine-6-phosphate deaminase 2 (GNPDA2), prolactin (PRL), brain-derived neurotrophic factor (BDNF), mitochondrial carrier homolog 2 (MTCH2), Fas apoptotic inhibitory molecule 2 (FAIM2), SH2B adaptor protein 1 (SH2B1), v-maf musculoaponeurotic fibrosarcoma oncogene homolog (MAF), Niemann-Pick disease, type C1 (NPC1), melanocortin 4 receptor (MC4R) and potassium channel tetramerisation domain containing 15 (KCTD15).]. 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:19851340; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP90106.RALGbF8DE61o7SPBwvvByneqlxIiEgKnM3XapgL8Jvkbw130_publicationInfo { this: dcterms:created "2015-08-25T14:38:29+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }