@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_head {
  this: np:hasAssertion dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_assertion;
    np:hasProvenance dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_provenance;
    np:hasPublicationInfo dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_assertion a np:Assertion .
  
  dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_provenance a np:Provenance .
  
  dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGN2b7ec5ff13d7c6631afc2c3afbd5d3df sio:SIO_000628 miriam-gene:1543, lld:C0014175;
    a sio:SIO_001121 .
}

dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_provenance {
  dgn-np:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_assertion dcterms:description
      "[The combination of CYP1A1 m1 polymorphism and GSTM1 null deletion is closely associated with penetration of the endometriosis phenotype, whereas GSTT1 null deletion may add to the penetration of this trait.]. 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:11730751;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP339310.RANLXEbg_lw-XlcrHoUvPN2l2M2XhpSY32u-BKN6dvg9k130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:55+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}