@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ> .
@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:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_head {
  this: np:hasAssertion dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion;
    np:hasProvenance dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance;
    np:hasPublicationInfo dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion a np:Assertion .
  
  dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance a np:Provenance .
  
  dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0349639 a ncit:C7057 .
  
  dgn-gda:DGN253a80f27fd113d37226b6b5dfdcc026 sio:SIO_000628 miriam-gene:7157, lld:C0349639;
    a sio:SIO_001121 .
}

dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance {
  dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion dcterms:description
      "[These data indicate that abnormalities of the p53 gene are rare in JMML and not responsible for acute transformation, but could be involved in the pathogenesis of some cases of JMML.]. 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:10520001;
    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:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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>,
      <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" .
}