@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs> .
@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:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_head {
  this: np:hasAssertion dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_assertion;
    np:hasProvenance dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_provenance;
    np:hasPublicationInfo dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_assertion a np:Assertion .
  
  dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_provenance a np:Provenance .
  
  dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0019829 a ncit:C7057 .
  
  dgn-gda:DGN7050e2c545f614fcc95f77246aae4443 sio:SIO_000628 miriam-gene:7157, lld:C0019829;
    a sio:SIO_001121 .
}

dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_provenance {
  dgn-np:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_assertion dcterms:description
      "[As the incidence of p53 mutations is significantly lower in Hodgkin's lymphoma than in other neoplasias, we investigated whether the malfunction of other proteins in this pathway could be responsible for its inactivation.]. 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:11839577;
    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:NP224841.RAAd0lzc0v0cwW9dxjs2bzFkTjTgYPnYevRktTAOVvirs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}