@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I> .
@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:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_head {
  this: np:hasAssertion dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_assertion;
    np:hasProvenance dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_provenance;
    np:hasPublicationInfo dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_assertion a np:Assertion .
  
  dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_provenance a np:Provenance .
  
  dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_assertion {
  miriam-gene:80350 a ncit:C16612 .
  
  lld:C0156344 a ncit:C7057 .
  
  dgn-gda:DGN609bc4c5615f1f127993aa0c146478f5 sio:SIO_000628 miriam-gene:80350, lld:C0156344;
    a sio:SIO_001121 .
}

dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_provenance {
  dgn-np:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_assertion dcterms:description
      "[We analyzed ovarian endometriosis lesions for loss of heterozygosity (LOH) at 12 loci of potential importance (D9S1870, D9S265, D9S270, D9S161, D11S29, D1S199, D8S261, APOA2, PTCH, TP53, D10S541, and D10S1765), including some at which genetic changes were previously reported in endometriosis.]. 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:15831286;
    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:NP949512.RAqfovUq3-n3DwXaDeh4xW8dDPK1d49JRe61HvlI4Iz_I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:19+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: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" .
}