@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4> .
@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:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_head {
  this: np:hasAssertion dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_assertion ;
    np:hasProvenance dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_provenance ;
    np:hasPublicationInfo dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_provenance a np:Provenance .
  dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_assertion {
  miriam-gene:4141 a ncit:C16612 .
  lld:C0600139 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_provenance {
  dgn-np:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_assertion dcterms:description "[Using the genomic DNA collected in a CaP case-control study (557 cases and 547 controls), we pilot tested the interactions of nine functionally characterized SNPs of three cytokine genes in CaP risk using the multivariate adaptive regression splines (MARS)-logit models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP816090.RA50AwKuqgIgXxSyy62azYf2WaXqeewfd-Wud0IKb9zH4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:20+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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