@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y> .
@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:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_head {
  this: np:hasAssertion dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_assertion;
    np:hasProvenance dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_provenance;
    np:hasPublicationInfo dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_assertion a np:Assertion .
  
  dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_provenance a np:Provenance .
  
  dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_assertion {
  miriam-gene:3119 a ncit:C16612 .
  
  lld:C0851578 a ncit:C7057 .
  
  dgn-gda:DGNe21ce23a73b58f43f8d546505021ba1c sio:SIO_000628 miriam-gene:3119, lld:C0851578;
    a sio:SIO_001122 .
}

dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_provenance {
  dgn-np:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_assertion dcterms:description
      "[The ICSD-2 was easily applicable in cases with typical cataplexy. In these cases, the MSLT and further evaluations were almost always positive and may thus not always be needed. Many patients without cataplexy were difficult to classify because of difficulties in interpreting the MSLT in the presence of sleep apnea or reduced sleep.]. 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:17162989;
    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:NP64940.RA9i2OjhOBYTJi61eBwkz2oveiAPELHAW17AmeSar6x9Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}