@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M> .
@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:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_head {
  this: np:hasAssertion dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_assertion;
    np:hasProvenance dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_provenance;
    np:hasPublicationInfo dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_assertion a np:Assertion .
  
  dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_provenance a np:Provenance .
  
  dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN65220517a7a1ef19de09478b6737150a sio:SIO_000628 miriam-gene:7157, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_provenance {
  dgn-np:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_assertion dcterms:description
      "[A total of 288 acute leukemia cases comprising 147 acute lymphocytic leukemia (ALL) and 141 acute myeloid leukemia (AML), as well as 245 controls were recruited for analysis of the TP53 72 polymorphism using PCR-RFLP method.]. 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:22502699;
    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:NP246619.RA2ARsms-FYz5f3_Aehv3UmdZ2hMYfGDLIvSlvt1cfj-M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}