@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA> .
@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:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_head {
  this: np:hasAssertion dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_assertion ;
    np:hasProvenance dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_provenance ;
    np:hasPublicationInfo dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_assertion a np:Assertion .
  dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_provenance a np:Provenance .
  dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  lld:C0346163 a ncit:C7057 .
  dgn-gda:DGN7e4479d997effe53b7ca3cb5ca8fe19b sio:SIO_000628 miriam-gene:5728 , lld:C0346163 ;
    a sio:SIO_001121 .
}
dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_provenance {
  dgn-np:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_assertion dcterms:description "[To investigate the potential role of the PTEN gene in the carcinogenesis of ovarian endometrioid carcinoma and its related subtype, clear cell carcinoma, we examined 20 ovarian endometrioid carcinomas, 24 clear cell carcinomas, and 34 solitary endometrial cysts of the ovary for LOH at 10q23.3 and point mutations within the entire coding region of the PTEN gene.]. 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:11156411 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP893738.RAnpIFn2X0iEqOFmMbHx40AqcMznXWDzVowasv7UBA4qA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}