@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc> .
@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:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_head {
  this: np:hasAssertion dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_assertion ;
    np:hasProvenance dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_provenance ;
    np:hasPublicationInfo dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_assertion a np:Assertion .
  dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_provenance a np:Provenance .
  dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_assertion {
  miriam-gene:1594 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_provenance {
  dgn-np:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_assertion dcterms:description "[A multivariate analysis revealed that the VDR FF genotype, family history of myocardial infarction, high body mass index at age 40, long working hours, and working with night shift to be independent potent risk factors for OPLL.]. 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:18628697 ;
    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:NP868710.RA-EqbrBBIGdhzanwayr8gUndQZU5Wa3C_dAvMPD8gjcc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:51+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 ;
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}