@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0> .
@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:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_head {
  this: np:hasAssertion dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion;
    np:hasProvenance dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance;
    np:hasPublicationInfo dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion a np:Assertion .
  
  dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance a np:Provenance .
  
  dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion {
  miriam-gene:1576 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN217aac7ac69e6bc7844ec387b6121584 sio:SIO_000628 miriam-gene:1576, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance {
  dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_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;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:15634941;
    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:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_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;
    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" .
}