@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g> .
@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:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_head {
  this: np:hasAssertion dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_assertion ;
    np:hasProvenance dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_provenance ;
    np:hasPublicationInfo dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_assertion a np:Assertion .
  dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_provenance a np:Provenance .
  dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_assertion {
  miriam-gene:154 a ncit:C16612 .
  lld:C0018802 a ncit:C7057 .
  dgn-gda:DGN19c50c7be5e1189cb5054b1c53885a22 sio:SIO_000628 miriam-gene:154 , lld:C0018802 ;
    a sio:SIO_001121 .
}
dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_provenance {
  dgn-np:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_assertion dcterms:description "[These data suggest that genetic variation of the ADRB2 is associated with differences in PF in CHF patients but not in healthy subjects, which may be related to an increased susceptibility of the homozygous Arg subjects to agonist-mediated desensitization of ADRB2s in the lungs, or related to an influence of this polymorphism on cardiac diastolic properties.]. 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:17099033 ;
    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:NP348075.RAFEa3WRRPNm8MwNNzta8ElpmybVHvJPRDyoLa8CvLI7g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:24+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" .
}