@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8> .
@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/v4.0.0/void/> .

dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_head {
  this: np:hasAssertion dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_assertion;
    np:hasProvenance dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_provenance;
    np:hasPublicationInfo dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_assertion a np:Assertion .
  
  dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_provenance a np:Provenance .
  
  dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_assertion {
  miriam-gene:8973 a ncit:C16612 .
  
  lld:C0028043 a ncit:C7057 .
  
  dgn-gda:DGNa7720dd2bcab319481ae20eca9512072 sio:SIO_000628 miriam-gene:8973, lld:C0028043;
    a sio:SIO_001121 .
}

dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_provenance {
  dgn-np:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_assertion dcterms:description
      "[We previously undertook pooled sequencing of the coding regions and flanking sequence of the CHRNA5, CHRNA3, CHRNB4, CHRNA6 and CHRNB3 genes and found that rare missense variants at conserved residues in CHRNB4 are associated with reduced risk of nicotine dependence among African Americans.]. 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:24804708;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1180169.RA3gYPxa1NQUJp_0kpFSO8gCj11iF87DfJjeLsuY0MzH8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:40+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 <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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}