@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_head {
  this: np:hasAssertion dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_assertion ;
    np:hasProvenance dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_provenance ;
    np:hasPublicationInfo dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_provenance a np:Provenance .
  dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_assertion {
  miriam-gene:9575 a ncit:C16612 .
  lld:C0525045 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_provenance {
  dgn-np:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_assertion dcterms:description "[In this view, and given the similarities between the circadian system of humans and rodents, it is expected that mutations of clock genes in humans may give rise to health problems, in particular sleep and mood disorders.]. 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:12791440 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP826921.RAnrNMRTpOLlxYhIVeYunwW-Qz7lV5MwQbvXIV43o59DE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:01+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}