@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU> .
@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:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_head {
  this: np:hasAssertion dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion;
    np:hasProvenance dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance;
    np:hasPublicationInfo dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion a np:Assertion .
  
  dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance a np:Provenance .
  
  dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0041408 a ncit:C7057 .
  
  dgn-gda:DGN6a828b53ab3c074b2aa339cedc173940 sio:SIO_000628 miriam-gene:7157, lld:C0041408;
    a sio:SIO_001121 .
}

dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance {
  dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion dcterms:description
      "[This observation may correlate with the involvement of the p53 protein in spermatogenesis, with its role in aneuploidy in cancer, and with the occurrence of two cases of Turner syndrome in families with germline TP53 mutations reported in the literature.]. 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:21665182;
    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:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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" .
}