@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4> .
@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:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_head {
  this: np:hasAssertion dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_assertion;
    np:hasProvenance dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_provenance;
    np:hasPublicationInfo dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_assertion a np:Assertion .
  
  dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_provenance a np:Provenance .
  
  dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_assertion {
  miriam-gene:2550 a ncit:C16612 .
  
  lld:C0037315 a ncit:C7057 .
  
  dgn-gda:DGN2e6a123431e248fe050d279edba584fa sio:SIO_000628 miriam-gene:2550, lld:C0037315;
    a sio:SIO_001122 .
}

dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_provenance {
  dgn-np:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_assertion dcterms:description
      "[The C/C variant of the Phe658Phe polymorphism GABA(B)R1 gene seems associated with the occurrence of OSAS and is also associated with some sleep related parameters (apnea arousal index and percent total sleep time in non-REM) recorded by polysomnography.]. 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:17264536;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP64651.RA4mLvYHoiso6CFTrtpQ4y1AfIlTgUxKFH3SOl6lGJ6V4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}