@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI> .
@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:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_head {
  this: np:hasAssertion dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_assertion;
    np:hasProvenance dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_provenance;
    np:hasPublicationInfo dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_assertion a np:Assertion .
  
  dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_provenance a np:Provenance .
  
  dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_assertion {
  miriam-gene:10383 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNed6eb069a8e7e5321b6fd808c6edde59 sio:SIO_000628 miriam-gene:10383, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_provenance {
  dgn-np:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_assertion dcterms:description
      "[The beta2-adrenergic receptor genotypes and haplotypes showed no modifying effects on these relationships or on the prevalence of dyslipidemia, diabetes, and coronary heart disease, yet, for all three polymorphisms, heterozygous carriers had a significantly lower relative risk for myocardial infarction (Arg-47Cys: n = 195, odds ratio (OR) = 0.32, P = 0.012; Arg16Gly: n = 197, OR = 0.39, P = 0.031; Gln27Glu: OR = 0.37, P = 0.023).]. 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:17198546;
    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:NP267481.RAatNL3ERtJ8dvxaXHWlje1ZbR125f-zPuPywZjvb0YJI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}