@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs> .
@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:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_head {
  this: np:hasAssertion dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion;
    np:hasProvenance dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance;
    np:hasPublicationInfo dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion a np:Assertion .
  
  dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance a np:Provenance .
  
  dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion {
  miriam-gene:5530 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNbbbdc80288c484e186403df68f69712d sio:SIO_000628 miriam-gene:5530, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance {
  dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion dcterms:description
      "[This study aimed to validate matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS)/Taqman copy number assay (CNA) CYP2D6 genotyping by AmpliChip CYP450 Test for the prediction of tamoxifen metabolizer phenotypes in breast cancer, and to investigate the influence of CYP2D6 variant coverage on genotype-phenotype relationships and tamoxifen outcome.]. 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:20515869;
    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:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:21+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" .
}