@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8> .
@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:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_head {
  this: np:hasAssertion dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion;
    np:hasProvenance dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance;
    np:hasPublicationInfo dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion a np:Assertion .
  
  dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance a np:Provenance .
  
  dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion {
  miriam-gene:154 a ncit:C16612 .
  
  lld:C0039494 a ncit:C7057 .
  
  dgn-gda:DGN08d7168e93e3eb95d7aec29448ef0d79 sio:SIO_000628 miriam-gene:154, lld:C0039494;
    a sio:SIO_001121 .
}

dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance {
  dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion dcterms:description
      "[Individuals who carried one haplotype coding for high and one coding for low ADRB2 expression displayed the highest positive psychological traits, had higher levels of resting arterial pressure, and were about 10 times less likely to develop TMD.]. 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:16741943;
    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:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:02+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" .
}