@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs> .
@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:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_head {
  this: np:hasAssertion dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion;
    np:hasProvenance dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_provenance;
    np:hasPublicationInfo dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion a np:Assertion .
  
  dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_provenance a np:Provenance .
  
  dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion {
  miriam-gene:3459 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN22622b41a1c19c2b4655fc1f9da52e9a sio:SIO_000628 miriam-gene:3459, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_provenance {
  dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion dcterms:description
      "[We have used a stepwise approach consisting of initial interrogation, confirmation and fine mapping to analyze STAT3, IL1B and IFNGR1 as modifiers of cystic fibrosis disease building upon the data and sample collection of the European Cystic Fibrosis Twin and Sibling 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:21731057;
    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:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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" .
}