@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo> .
@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:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_head {
  this: np:hasAssertion dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion;
    np:hasProvenance dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance;
    np:hasPublicationInfo dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion a np:Assertion .
  
  dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance a np:Provenance .
  
  dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN62e1cc25f6a08f96ba0fb3bc2709d3ff sio:SIO_000628 miriam-gene:5925, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance {
  dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion dcterms:description
      "[In order to address a possible role for the human retinoblastoma susceptibility (RB1) gene in hematopoietic malignancies, 34 cases of different types of leukemia without chromosomal abnormalities at band 13q14 were analyzed by Southern blot hybridization.]. 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:1884351;
    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:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}