@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ> .
@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:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_head {
  this: np:hasAssertion dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion ;
    np:hasProvenance dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion a np:Assertion .
  dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance a np:Provenance .
  dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion {
  miriam-gene:4988 a ncit:C16612 .
  lld:C0600241 a ncit:C7057 .
  dgn-gda:DGN2f87a7783ecdfdbe239e4b9060fe763a sio:SIO_000628 miriam-gene:4988 , lld:C0600241 ;
    a sio:SIO_001122 .
}
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance {
  dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion dcterms:description "[For the A118G polymorphism, we found significant differences in allele and genotype frequencies between different ethnic groups and highly significant association with heroin dependence in Indians for both genotype distribution (p = 0.024) and allele frequency (p = 0.009). For the C17 T polymorphism, the minor allele was documented in Chinese and Malays for the first time. Molecular haplotyping revealed complete linkage dis-equilibrium between the A118G and C17 T polymorphisms. Linkage disequilibrium between the A118G and C1031G polymorphisms was found to be almost complete in all four ethnic groups.]. 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:12657887 ;
    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:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}