@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc> .
@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:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_head {
  this: np:hasAssertion dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_assertion ;
    np:hasProvenance dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_provenance ;
    np:hasPublicationInfo dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_assertion a np:Assertion .
  dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_provenance a np:Provenance .
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}
dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_assertion {
  miriam-gene:1136 a ncit:C16612 .
  lld:C0028043 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_provenance {
  dgn-np:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_assertion dcterms:description "[The purpose of this study was to analyse the association of smoking status and smoking-related phenotypes (included nicotine dependence) with 17 candidate genetic variants: CYP2A6*1×2, CYP2A6*2 (1799T>A) [rs1801272], CYP2A6*9 (-48T>G) [rs28399433], CYP2A6*12, CYP2A13*2 (3375C>T) [rs8192789], CYP2A13*3 (7520C>G), CYP2A13*4 (579G>A), CYP2A13*7 (578C>T) [rs72552266], CYP2B6*4 (785A>G), CYP2B6*9 (516G>T), CHRNA3 546C>T [rs578776], CHRNA5 1192G>A [rs16969968], CNR1 3764C>G [rs6928499], DRD2-ANKK1 2137G>A (Taq1A) [rs1800497], 5HTT LPR, HTR2A -1438A>G [rs6311] and OPRM1 118A>G [rs1799971].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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  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:NP268158.RAB-FrlMCKHzFn4powuplQ0GxbfbJF5xNYxlkrkixquZc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+02:00"^^xsd:dateTime ;
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