@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_head {
   this: np:hasAssertion dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_assertion ;
    np:hasProvenance dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_provenance ;
    np:hasPublicationInfo dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_assertion a np:Assertion .
  dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_provenance a np:Provenance .
  dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_assertion {
   miriam-gene:1573 a ncit:C16612 .
  lld:C0149654 a ncit:C7057 .
  dgn-gda:DGNc04eb9f4bef7403d2df89e1c0af18b23 sio:SIO_000628 miriam-gene:1573 , lld:C0149654 ;
    a sio:SIO_001122 .
}
dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_provenance {
   dgn-np:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_assertion dcterms:description "[ The CYP2J2*7 variant represents a relatively rare polymorphism in Chinese, with the allele frequency being comparable to that of Korean, but significantly lower than those of African and White groups. This data may be informative to design population-bas]. 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:16182271 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP54746.RACQdbocoKf1-P0IuIvll7SXMPDqQplpM1LUPH91xa4Qw130_publicationInfo {
   this: dcterms:created "2015-08-25T14:38:10+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:disgenetv3.0rdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}