@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_head {
  this: np:hasAssertion dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_assertion;
    np:hasProvenance dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_provenance;
    np:hasPublicationInfo dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_assertion a np:Assertion .
  
  dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_provenance a np:Provenance .
  
  dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_assertion {
  miriam-gene:54658 a ncit:C16612 .
  
  lld:C0017551 a ncit:C7057 .
  
  dgn-gda:DGNba6472ac5b626d4673d107c9d320deee sio:SIO_000628 miriam-gene:54658, lld:C0017551;
    a sio:SIO_001122 .
}

dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_provenance {
  dgn-np:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_assertion dcterms:description
      "[ The method we set up is suitable for the detection of UGT 1A1 polymorphism in routine practice before irinotecan treatment. It could help to detect the patients homozygous or heterozygous for Gilbert's syndrome, at-risk of CPT 11-induced toxicity, and th]. 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:15297419;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP80632.RAeA66k_NRPxle90rLj0sS2pqX6ysUom9fVobdmZ95J3M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:24+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}