@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q> .
@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:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_head {
  this: np:hasAssertion dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion;
    np:hasProvenance dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance;
    np:hasPublicationInfo dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion a np:Assertion .
  
  dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance a np:Provenance .
  
  dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion {
  miriam-gene:1499 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGNadb34b8cf48ccd1093737c5de90939aa sio:SIO_000628 miriam-gene:1499, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance {
  dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion dcterms:description
      "[Mutations in the beta-catenin (CTNNB1) gene have been recently reported in a small percentage of UECs and in the endometrioid variant of ovarian carcinoma suggesting that the Wnt signal transduction pathway is involved in the development of female genital tract tumors with endometrioid morphology.]. 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:11048799;
    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:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}