@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs> .
@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:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_head {
  this: np:hasAssertion dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_assertion;
    np:hasProvenance dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_provenance;
    np:hasPublicationInfo dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_assertion a np:Assertion .
  
  dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_provenance a np:Provenance .
  
  dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_assertion {
  miriam-gene:3930 a ncit:C16612 .
  
  lld:C0005859 a ncit:C7057 .
  
  dgn-gda:DGN210bbfbe3f60b90554e3c38cfb6ab282 sio:SIO_000628 miriam-gene:3930, lld:C0005859;
    a sio:SIO_001121 .
}

dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_provenance {
  dgn-np:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_assertion dcterms:description
      "[Even though PHA-stimulated BS lymphocytes from all five patients studied showed high levels of sister chromatid exchange (SCE), three EBV-transformed BS-B-lymphoid cell lines had normal levels of SCE and two yielded two types of cell populations, i.e., one with increased SCE and chromosome instability (including breaks and quadriradials) and another with normal levels of SCE and without structural aberrations.]. 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:6303556;
    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:NP783750.RA2cyWRAyiMPtzAF1IkPcu1PcjI139jrjqLkBkSXw2KSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:54+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" .
}