@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM> .
@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:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_head {
  this: np:hasAssertion dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_assertion;
    np:hasProvenance dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_provenance;
    np:hasPublicationInfo dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_assertion a np:Assertion .
  
  dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_provenance a np:Provenance .
  
  dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0019829 a ncit:C7057 .
  
  dgn-gda:DGN3327c64f9245ac2ebfa9bc87431cea7a sio:SIO_000628 miriam-gene:7157, lld:C0019829;
    a sio:SIO_001121 .
}

dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_provenance {
  dgn-np:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_assertion dcterms:description
      "[p53 was also strongly expressed in the nuclei of Reed Sternberg cells from 19 of 37 cases of Hodgkin's disease, including six cases of mixed cellularity, and 13 cases of nodular sclerosing type.]. 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:1466398;
    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:NP296210.RAA1YQr5qKZR-0ewaTpxVpAd1FQaGd-r5KlNBMu0y4oOM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}