@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c> .
@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:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_head {
  this: np:hasAssertion dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_assertion;
    np:hasProvenance dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_provenance;
    np:hasPublicationInfo dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_assertion a np:Assertion .
  
  dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_provenance a np:Provenance .
  
  dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_assertion {
  miriam-gene:1140 a ncit:C16612 .
  
  lld:C0028043 a ncit:C7057 .
  
  dgn-gda:DGN85e1b8b3a4d711c37ce9dc0349ae504c sio:SIO_000628 miriam-gene:1140, lld:C0028043;
    a sio:SIO_001121 .
}

dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_provenance {
  dgn-np:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_assertion dcterms:description
      "[We found evidence that genetic variation at CHRNA1, CHRNA2, CHRNA7, and CHRNB1 alters susceptibility to nicotine dependence, but we did not replicate any of the most significant single nucleotide polymorphism associations from the NICSNP high-density association study.]. 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:19307444;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  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:NP858152.RAvJgl8eOr_agYdoCFVdKVfsx6Ts3Gj_eQPquir3v9Y_c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}