@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM> .
@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:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_head {
   this: np:hasAssertion dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_assertion ;
    np:hasProvenance dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_provenance ;
    np:hasPublicationInfo dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_assertion a np:Assertion .
  dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_provenance a np:Provenance .
  dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_assertion {
   miriam-gene:1828 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
  dgn-gda:DGNff994e27362bfbbc582fd8cf6a59dd29 sio:SIO_000628 miriam-gene:1828 , lld:C0011849 ;
    a sio:SIO_001121 .
}
dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_provenance {
   dgn-np:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_assertion dcterms:description "[To search for sequence variants that affect variation in two common measures of obesity, weight and body mass index (BMI), both of which are highly heritable, we performed a genome-wide association (GWA) study with 305,846 SNPs typed in 25,344 Icelandic, 2,998 Dutch, 1,890 European Americans and 1,160 African American subjects and combined the results with previously published results from the Diabetes Genetics Initiative (DGI) on 3,024 Scandinavians.]. 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:19079260 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP187641.RAXSi9Y302GO9ilkD_juxcPBweZJdz-txXVCF9Q2-7wrM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:43+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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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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