@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38> .
@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:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_head {
  this: np:hasAssertion dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion;
    np:hasProvenance dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_provenance;
    np:hasPublicationInfo dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion a np:Assertion .
  
  dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_provenance a np:Provenance .
  
  dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion {
  miriam-gene:6774 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
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dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_provenance {
  dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion dcterms:description
      "[Our results indicate that genetic variants in STAT3, independent of asthma treatment, are determinants of FEV1 in both adults and children with asthma, and suggest that STAT3 may participate in inflammatory pathways that have an impact on level of lung function.]. 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:15935090;
    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:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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