@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ> .
@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:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_head {
  this: np:hasAssertion dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_assertion;
    np:hasProvenance dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_provenance;
    np:hasPublicationInfo dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_assertion a np:Assertion .
  
  dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_provenance a np:Provenance .
  
  dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0027498 a ncit:C7057 .
  
  dgn-gda:DGN925fede4fbdfd1477c4d8665968319f2 sio:SIO_000628 miriam-gene:5243, lld:C0027498;
    a sio:SIO_001121 .
}

dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_provenance {
  dgn-np:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_assertion dcterms:description
      "[Our study shows that in Indonesian cancer patients treated with highly cytostatic emetogenic, carriership of the CTG haplotype of the ABCB1 gene is related to an increased risk of delayed chemotherapy-induced nausea and vomiting.]. 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:21840870;
    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:NP682279.RAzS3tE9ZZ0ZyiDc2pKnSBeeHpLLpTMHSw3EoreBDNycQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:54+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" .
}