@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo> .
@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:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_head {
  this: np:hasAssertion dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_assertion;
    np:hasProvenance dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_provenance;
    np:hasPublicationInfo dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_assertion a np:Assertion .
  
  dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_provenance a np:Provenance .
  
  dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_assertion {
  miriam-gene:8101 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN600b68e216cb88aa375edc2a996303a6 sio:SIO_000628 miriam-gene:8101, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_provenance {
  dgn-np:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_assertion dcterms:description
      "[We investigated loci known to play a role in the genesis or disease progression of other subtypes of lymphoid malignancies, namely the P53 gene (17p13), the retinoblastoma gene (RB, 13q14), the D13S25 locus (13q14), and the P16(INK4A) gene (9p21).]. 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:10913669;
    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:NP862398.RABKatwzq4acOjkOoZ29VdrDqPiFZQ2vboC7Sw_p9-_lo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}