@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:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_head { this: np:hasAssertion dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_assertion; np:hasProvenance dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_provenance; np:hasPublicationInfo dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_publicationInfo; a np:Nanopublication . dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_assertion a np:Assertion . dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_provenance a np:Provenance . dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_publicationInfo a np:PublicationInfo . } dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_assertion { miriam-gene:4160 a ncit:C16612 . lld:C0497406 a ncit:C7057 . dgn-gda:DGNf613333bd0d379e8a8a91fb8b1b7a93d sio:SIO_000628 miriam-gene:4160, lld:C0497406; a sio:SIO_001122 . } dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_provenance { dgn-np:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_assertion dcterms:description "[MC4R variants were detected in three patients: the known I169S variant was found in heterozygote state in two patients and a novel heterozygous Y302F mutation was detected in one 12-year-old girl (BMI = 34 kg/m(2), BMI z-score 2.7) who has been overweight since the second year of life and suffered from hyperinsulinemia (at the age of 12: fasting insulin 45 mU/ml, after oral glucose load max.]. 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:19214805; 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:NP720389.RAj-ua0nLAc_69PpLJqnsGh88UXLsMGMRQQkNeqP0GKAE130_publicationInfo { this: dcterms:created "2016-05-13T12:47:11+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" . }