@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w> .
@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:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_head {
  this: np:hasAssertion dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_assertion;
    np:hasProvenance dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_provenance;
    np:hasPublicationInfo dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_assertion a np:Assertion .
  
  dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_provenance a np:Provenance .
  
  dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_assertion {
  miriam-gene:3251 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGN079db672e0effc8388f14db9dba6ba1d sio:SIO_000628 miriam-gene:3251, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_provenance {
  dgn-np:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_assertion dcterms:description
      "[The most often studied genotoxicity endpoints have been selected for inclusion in this document and they are structural and numerical chromosomal aberrations assessed using cytogenetic methods (classical chromosomal aberration analysis (CA), fluorescence in situ hybridisation (FISH), micronuclei (MN)); DNA damage (adducts, strand breaks, crosslinking, alkali-labile sites) assessed using bio-chemical/electrophoretic assays or sister chromatid exchanges (SCE); protein adducts; and hypoxanthine-guanine phosphoribosyltransferase (HPRT) mutations.]. 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:10913908;
    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:NP363248.RAK7vHqCheSa8SIykSAkACaL0l_30gDExb_lR8lzLSg_w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:32+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" .
}