@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds> .
@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 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:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_head {
   this: np:hasAssertion dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_assertion ;
    np:hasProvenance dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_provenance ;
    np:hasPublicationInfo dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_assertion a np:Assertion .
  dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_provenance a np:Provenance .
  dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_assertion {
   miriam-gene:7399 a ncit:C16612 .
  lld:C0040336 a ncit:C7057 .
  dgn-gda:DGNcdf7a7fb12453c1ed36037771a399924 sio:SIO_000628 miriam-gene:7399 , lld:C0040336 ;
    a sio:SIO_001122 .
}
dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_provenance {
   dgn-np:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_assertion dct:description "[These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. 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:18519826 ;
    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:NP79977.RA8PbCvdNe-122iDa7hbZXVbZOW7Qr6Q11fkEdqT4sAds130_publicationInfo {
   this: dct:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}