@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI> .
@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:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_head {
  this: np:hasAssertion dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_assertion;
    np:hasProvenance dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_provenance;
    np:hasPublicationInfo dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_assertion a np:Assertion .
  
  dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_provenance a np:Provenance .
  
  dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0206638 a ncit:C7057 .
  
  dgn-gda:DGN7a7de481597df278ba42169030fae2bb sio:SIO_000628 miriam-gene:7157, lld:C0206638;
    a sio:SIO_001121 .
}

dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_provenance {
  dgn-np:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_assertion dcterms:description
      "[We examined 43 cases of GCTB (38 conventional cases, two lung implantation cases, and three secondary malignant cases) for p53 gene mutations and for loss of heterozygosity (LOH) of p53 when corresponding normal tissue was available.]. 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:23748877;
    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:NP171974.RA4vSpPNzsBTJbTnhL3zZKMSJM853570onMASJZryd-mI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}