@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs> .
@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:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_head {
  this: np:hasAssertion dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion;
    np:hasProvenance dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance;
    np:hasPublicationInfo dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion a np:Assertion .
  
  dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance a np:Provenance .
  
  dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGN97dd2fbeff2526fa3491e88b1fa2e644 sio:SIO_000628 miriam-gene:7157, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance {
  dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion dcterms:description
      "[p53 gene mutations are rarely detected at diagnosis in common haematological cancers such as multiple myeloma (MM), acute myeloid leukaemia (AML), chronic lymphocytic leukaemia (CLL) and Hodgkin's disease (HD), although their prevalence may increase with progression to more aggressive or advanced stages.]. 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:19955555;
    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:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}