@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg> .
@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:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_head {
  this: np:hasAssertion dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion;
    np:hasProvenance dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance;
    np:hasPublicationInfo dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion a np:Assertion .
  
  dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance a np:Provenance .
  
  dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0751623 a ncit:C7057 .
  
  dgn-gda:DGN6f02f8ba6aab7ec46392d1cd3dc90f92 sio:SIO_000628 miriam-gene:7157, lld:C0751623;
    a sio:SIO_001121 .
}

dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance {
  dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion dcterms:description
      "[We investigated the possibility that p53 mutations in the germline are associated with second primary cancers that arise in children and young adults who would not be considered as belonging to Li-Fraumeni families.]. 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:1565144;
    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:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}