@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0> .
@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:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_head {
  this: np:hasAssertion dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_assertion;
    np:hasProvenance dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_provenance;
    np:hasPublicationInfo dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_assertion a np:Assertion .
  
  dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_provenance a np:Provenance .
  
  dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_assertion {
  miriam-gene:51639 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN0861945e4968b647ade9c8f196ed8a3e sio:SIO_000628 miriam-gene:51639, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_provenance {
  dgn-np:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_assertion dcterms:description
      "[Testing by qPCR of 18 bone marrow specimens from paediatric acute lymphoblastic leukaemia (ALL) patients at diagnosis revealed nine to be GG, six to be GD and three to be DD for exon 2 of p14(ARF)/p16(INK4A), concordant with Southern blotting analysis.]. 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:15607365;
    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:NP887504.RAYrsU5BLduxIk9nBErk7-CTeMowfYM4RLiaMCHMjUWG0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:05+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" .
}