@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0> .
@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:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_head {
  this: np:hasAssertion dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_assertion ;
    np:hasProvenance dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_provenance ;
    np:hasPublicationInfo dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_assertion a np:Assertion .
  dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_provenance a np:Provenance .
  dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_assertion {
  miriam-gene:23120 a ncit:C16612 .
  lld:C0035204 a ncit:C7057 .
  dgn-gda:DGN181fd67f21fce2ea88673df5a34f9437 sio:SIO_000628 miriam-gene:23120 , lld:C0035204 ;
    a sio:SIO_001122 .
}
dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_provenance {
  dgn-np:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_assertion dcterms:description "[This analysis confirms prior reports of significant heritability of sleepiness, usual bedtime, and usual sleep duration. Several genetic loci with suggestive linkage to these traits are identified, including linkage peaks containing circadian clock-related genes. Association tests identify NPSR1 and PDE4D as possible mediators of bedtime and sleepiness.]. 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:17903308 ;
    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:NP94138.RACOD9EiI0dER6TCIOs7YLpngf4mSB8rC0Zf3c09_8hq0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}