@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo> .
@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:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_head {
  this: np:hasAssertion dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_assertion ;
    np:hasProvenance dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_provenance ;
    np:hasPublicationInfo dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_assertion a np:Assertion .
  dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_provenance a np:Provenance .
  dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  lld:C0023895 a ncit:C7057 .
  dgn-gda:DGN9af45ac63ba23125afb53085c6b67d00 sio:SIO_000628 miriam-gene:1557 , lld:C0023895 ;
    a sio:SIO_001121 .
}
dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_provenance {
  dgn-np:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_assertion dcterms:description "[A polymorphic CYP2C19 gene was analyzed in 233 Japanese subjects, including 63 with Parkinson's disease, 92 with chronic liver diseases (35 chronic hepatitis, 19 liver cirrhosis, 16 hepatocellular carcinoma, 10 primary biliary cirrhosis and 12 autoimmune hepatitis), 14 with lung cancer (squamous cell carcinoma) and 64 healthy subjects to determine the genotype distributions of the CYP2C19 gene and to investigate its involvement in the diseases.]. 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:8890945 ;
    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:NP748360.RAB3LKtJeVmayl6FQT63v32sNlQAM5U79o1XyhxNNkJqo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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" .
}