@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ> .
@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/v4.0.0/void/> .
dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_head {
  this: np:hasAssertion dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_assertion ;
    np:hasProvenance dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_assertion a np:Assertion .
  dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_provenance a np:Provenance .
  dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  lld:C0014173 a ncit:C7057 .
  dgn-gda:DGN4848b36f7eed0a15c7437b07f40e18a9 sio:SIO_000628 miriam-gene:5624 , lld:C0014173 ;
    a sio:SIO_001121 .
}
dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_provenance {
  dgn-np:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_assertion dcterms:description "[Our results indicate that de novo mutation or loss of heterozygosity in stromal APC is sufficient to induce endometrial hyperplasia and endometrial carcinogenesis by mechanisms that are consistent with unopposed estrogen signaling in the endometrial epithelium.]. 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:21363919 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP876284.RArzX3voGKYTQ5tgOjcwoWiHkAIrRoU5H706XeFLexcmQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:21+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: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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}