@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg> .
@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:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_head {
  this: np:hasAssertion dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_assertion;
    np:hasProvenance dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_provenance;
    np:hasPublicationInfo dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_assertion a np:Assertion .
  
  dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_provenance a np:Provenance .
  
  dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_assertion {
  miriam-gene:373156 a ncit:C16612 .
  
  lld:C0220641 a ncit:C7057 .
  
  dgn-gda:DGNbe72997ed6243f2ef51877108fdcd48c sio:SIO_000628 miriam-gene:373156, lld:C0220641;
    a sio:SIO_001121 .
}

dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_provenance {
  dgn-np:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_assertion dcterms:description
      "[Here the mtDNA polymorphisms at 12,308 nucleotide pairs (np), 11,467 np, 10,400 np, and 10,398 np were studied to examine the association with the risk of oral cancer and leukoplakia, alone and in combination with polymorphisms at the GST loci.]. 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:17886251;
    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:NP336994.RAOYYQuL9EwwewfcLunGK_e16QJBn9N_WcRSv_VRVFoEg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}