@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog> .
@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:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_head {
  this: np:hasAssertion dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_assertion;
    np:hasProvenance dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_provenance;
    np:hasPublicationInfo dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_assertion a np:Assertion .
  
  dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_provenance a np:Provenance .
  
  dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_assertion {
  miriam-gene:2947 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGNf1862664f77e39f1543d9c5c14cd30fc sio:SIO_000628 miriam-gene:2947, lld:C0024623;
    a sio:SIO_001121 .
}

dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_provenance {
  dgn-np:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_assertion dcterms:description
      "[A case-control study was performed in 303 subjects (108 GC and 195 healthy controls) to analyze the association of polymorphisms in GSTM1, GSTT1, GSTP1, GSTM3, CYP1A1, and CYP2E1 genes in susceptibility to GC in Kashmir Valley.]. 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:19521675;
    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:NP376091.RAmHu8RsoPGjk9bqezFnRdW7nw4_HfxwEFAHuShKJzpog130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}