@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8> .
@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:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_head {
  this: np:hasAssertion dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_assertion;
    np:hasProvenance dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_provenance;
    np:hasPublicationInfo dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_assertion a np:Assertion .
  
  dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_provenance a np:Provenance .
  
  dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_assertion {
  miriam-gene:2052 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNd7ab8a7cd831cf5bca468662b1187808 sio:SIO_000628 miriam-gene:2052, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_provenance {
  dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_assertion dcterms:description
      "[In this study, we firstly aimed to investigate the relationship between EPHX1 Tyr113His and His139Arg variants, and the risk of incidence of childhood acute lymphoblastic leukemia (ALL) in Turkish population, comprised of 190 healthy controls and 167 ALL patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:21983886;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP14840.RAN6Vbb3TIzsQIPb3VzdtBgzrcPkl4FeCQi4HSjEmO2K8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:05+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" .
}