@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk> .
@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:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_head {
  this: np:hasAssertion dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_assertion ;
    np:hasProvenance dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_provenance ;
    np:hasPublicationInfo dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_assertion a np:Assertion .
  dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_provenance a np:Provenance .
  dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_assertion {
  miriam-gene:3479 a ncit:C16612 .
  lld:C0008679 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_provenance {
  dgn-np:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_assertion dcterms:description "[Multiple linear regression models were used to determine the extent to which sociodemographic characteristics, lifestyle factors, personal and family history of chronic disease, and common genetic variants, the (CA)n repeat polymorphism in the IGF1 promoter and the IGFBP3-202 A/C polymorphism (rs2854744) predict variation in IGF1 or IGFBP3 serum levels in 33 otherwise healthy African American and 37 white males recruited from Durham Veterans Administration Medical Center.]. 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:19634593 ;
    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:NP344474.RAVaXm5iuEPF9rKbYnhU7XmimdI62qu6wpjmpfazKmzOk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    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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}