@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_head {
  this: np:hasAssertion dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_assertion ;
    np:hasProvenance dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_provenance a np:Provenance .
  dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_assertion {
  miriam-gene:51141 a ncit:C16612 .
  lld:C0004153 a ncit:C7057 .
  dgn-gda:DGN42b5396bfe1e3293731f4196da34ca78 sio:SIO_000628 miriam-gene:51141 , lld:C0004153 ;
    a sio:SIO_001121 .
}
dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_provenance {
  dgn-np:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_assertion dcterms:description "[The goal of the study reported here was to assess the role of the INSIG2 single nucleotide polymorphism (SNP) in susceptibility to obesity in the prospective longitudinal Atherosclerosis Risk in Communities (ARIC) study (n = 14,566) and in three other cohorts: the Coronary Artery Risk Development in Young Adults (CARDIA) study (n = 3,888), the Genetic Epidemiology Network of Arteriopathy (GENOA) study (n = 4,766), and extremely obese and lean individuals ascertained at the University of Ottawa (n = 1,502).]. 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:19523229 ;
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  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:NP490959.RARXJDGgjDB4kxmckKjyw4WO-PdRsw_v0Xvbxs5M0G5HQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
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}