@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk> .
@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:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_head {
  this: np:hasAssertion dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_assertion;
    np:hasProvenance dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_provenance;
    np:hasPublicationInfo dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_assertion a np:Assertion .
  
  dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_provenance a np:Provenance .
  
  dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0017601 a ncit:C7057 .
  
  dgn-gda:DGN3b41a066a2190759b6c4278738ded7fe sio:SIO_000628 miriam-gene:2944, lld:C0017601;
    a sio:SIO_001121 .
}

dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_provenance {
  dgn-np:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_assertion dcterms:description
      "[We excluded patients and controls with cataract or past history of cataract surgery, asthma, past history of malignancy, cardiovascular disease that on medication and known cases of glaucoma, because these traits were associated with GSTM1 and/or GSTT1 polymorphisms.]. 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:21701824;
    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:NP813899.RAfCV2-f8lpf5ktGvz9mdHaHsIQ-so3kHP_aI0JiAbeCk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:19+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" .
}