@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4> .
@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:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_head {
  this: np:hasAssertion dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion ;
    np:hasProvenance dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance ;
    np:hasPublicationInfo dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion a np:Assertion .
  dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance a np:Provenance .
  dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion {
  miriam-gene:3658 a ncit:C16612 .
  lld:C0024117 a ncit:C7057 .
  dgn-gda:DGNb385944eefe626f4c015062e8ea6eb48 sio:SIO_000628 miriam-gene:3658 , lld:C0024117 ;
    a sio:SIO_001121 .
}
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance {
  dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion dcterms:description "[Genome-wide association studies and integrative genomics approaches in COPD have demonstrated significant associations with SNPs in the chromosome 15q region that includes CHRNA3 (cholinergic nicotine receptor alpha3) and IREB2 (iron regulatory binding protein 2).We investigated whether SNPs in the chromosome 15q region would be modifiers for lung function and COPD in AAT deficiency.]. 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:22356581 ;
    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:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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> ;
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}