@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc> .
@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:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_head {
   this: np:hasAssertion dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_assertion ;
    np:hasProvenance dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_provenance ;
    np:hasPublicationInfo dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_provenance a np:Provenance .
  dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_assertion {
   miriam-gene:7157 a ncit:C16612 .
  lld:C0014175 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_provenance {
   dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_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 ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP315860.RAQuqEPR95Dbxwey0DT4y5wbp3ovT5j_b2F5Hh6-uEAjc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:01+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}