@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s> .
@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:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_head {
  this: np:hasAssertion dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_assertion;
    np:hasProvenance dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_provenance;
    np:hasPublicationInfo dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_assertion a np:Assertion .
  
  dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_provenance a np:Provenance .
  
  dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0015625 a ncit:C7057 .
  
  dgn-gda:DGN363c7c30852b8573bc3c767f646eb34b sio:SIO_000628 miriam-gene:7157, lld:C0015625;
    a sio:SIO_001121 .
}

dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_provenance {
  dgn-np:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_assertion dcterms:description
      "[Using single strand conformation polymorphism analysis of PCR products, we looked for TP53 mutations in DNA of patients with Fanconi anemia, an autosomal recessive disease characterized by increased predisposition to neoplasia.]. 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:1803324;
    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:NP284929.RAr-ZUnASbjS48MSwJbp02Lu6WLURvddq_m0Km-xR008s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:40+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" .
}