@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI> .
@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:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_head {
  this: np:hasAssertion dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_assertion;
    np:hasProvenance dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_provenance;
    np:hasPublicationInfo dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_assertion a np:Assertion .
  
  dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_provenance a np:Provenance .
  
  dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0024305 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_provenance {
  dgn-np:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_assertion dcterms:description
      "[We conclude that the two polymorphisms, GSTT1 null and PON1 BB, are common genetic traits that pose low individual risk but may be important determinants of overall population NHL risk, particularly among groups exposed to NHL-related carcinogens.]. 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:12139735;
    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:NP694868.RAsXuemIPCBPEnCLG3VT9vD3ZfECHW17bFFhRvfre30DI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:02+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}