@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0> .
@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:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_head {
  this: np:hasAssertion dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion;
    np:hasProvenance dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance;
    np:hasPublicationInfo dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion a np:Assertion .
  
  dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance a np:Provenance .
  
  dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion {
  miriam-gene:5460 a ncit:C16612 .
  
  lld:C0007099 a ncit:C7057 .
  
  dgn-gda:DGNe0e51e9efdaf25ada8bea46d2be52131 sio:SIO_000628 miriam-gene:5460, lld:C0007099;
    a sio:SIO_001121 .
}

dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance {
  dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion dcterms:description
      "[Failure to switch off OCT4 in GC perinatally can lead to development of carcinoma in situ (CIS), the precursor of testicular germ cell cancer (TGCC), for which there is no animal model.]. 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:23321215;
    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:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:36+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" .
}