@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8> .
@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:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_head {
  this: np:hasAssertion dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion;
    np:hasProvenance dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance;
    np:hasPublicationInfo dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion a np:Assertion .
  
  dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance a np:Provenance .
  
  dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion {
  miriam-gene:5460 a ncit:C16612 .
  
  lld:C0855197 a ncit:C7057 .
  
  dgn-gda:DGN0bbd3be02abda7cd631e53123ab8c7ca sio:SIO_000628 miriam-gene:5460, lld:C0855197;
    a sio:SIO_001121 .
}

dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance {
  dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_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:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:35+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" .
}