@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U> .
@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:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_head {
  this: np:hasAssertion dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_assertion ;
    np:hasProvenance dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_provenance ;
    np:hasPublicationInfo dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_provenance a np:Provenance .
  dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_assertion {
  miriam-gene:1577 a ncit:C16612 .
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dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_provenance {
  dgn-np:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_assertion dcterms:description "[We predict that individuals who are homozygous for defective alleles of both of these genes would metabolize CYP3A substrates poorly. The new genetic tests will be useful in future clinical studies to investigate genotype/phenotype associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP60134.RAiphTP3looDt-10JECj0fy7DPAOZJBWyXPv3_E2tv53U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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