@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA> .
@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:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_head {
  this: np:hasAssertion dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_assertion ;
    np:hasProvenance dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_provenance ;
    np:hasPublicationInfo dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_assertion a np:Assertion .
  dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_provenance a np:Provenance .
  dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_assertion {
  miriam-gene:8289 a ncit:C16612 .
  lld:C0206687 a ncit:C7057 .
  dgn-gda:DGN4d987027cc4fba368ac4de10f280b956 sio:SIO_000628 miriam-gene:8289 , lld:C0206687 ;
    a sio:SIO_001121 .
}
dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_provenance {
  dgn-np:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_assertion dcterms:description "[Of the nine cases of complex atypical endometrial hyperplasia, all showed BAF250a expression; however, of 10 cases of atypical endometriosis (the putative precursor lesion for ovarian clear cell and endometrioid carcinoma), one case showed loss of staining for BAF250a in the atypical areas, with retention of staining in areas of non-atypical 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:21590771 ;
    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:NP895034.RAidvowQs00T1LIt_jtcrRc32Ht7z8kcfANLh_vSDMEFA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:30+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" .
}