@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI> .
@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:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_head {
  this: np:hasAssertion dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion;
    np:hasProvenance dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance;
    np:hasPublicationInfo dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion a np:Assertion .
  
  dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance a np:Provenance .
  
  dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion {
  miriam-gene:1298 a ncit:C16612 .
  
  lld:C0158266 a ncit:C7057 .
  
  dgn-gda:DGNe0e779ce79a4a4b7d97edc15c8d66015 sio:SIO_000628 miriam-gene:1298, lld:C0158266;
    a sio:SIO_001122 .
}

dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance {
  dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion dcterms:description
      "[ This largest-ever population study using MRI to define DDD demonstrates for the first time that the Trp2 allele is a significant risk factor for the development and severity of degeneration. The association is age- dependent as it is more prevalent in some age groups than in others. The contrasting Trp allele frequencies between the Finns and the Chinese are the first indication that the genetic risk factors for DDD varies between ethnic groups.]. 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:16371896;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}