@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0> .
@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:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_head {
  this: np:hasAssertion dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion;
    np:hasProvenance dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance;
    np:hasPublicationInfo dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion a np:Assertion .
  
  dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance a np:Provenance .
  
  dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion {
  miriam-gene:1588 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGN8a65c48c319c0e36b76846bae2f1573e sio:SIO_000628 miriam-gene:1588, lld:C0014175;
    a sio:SIO_001122 .
}

dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance {
  dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion dcterms:description
      "[ Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. 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:12620480;
    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:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_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" .
}