@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0> .
@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:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_head {
  this: np:hasAssertion dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion;
    np:hasProvenance dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance;
    np:hasPublicationInfo dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion a np:Assertion .
  
  dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance a np:Provenance .
  
  dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0009207 a ncit:C7057 .
  
  dgn-gda:DGN967592696bd321ec6729aa756391715b sio:SIO_000628 miriam-gene:5621, lld:C0009207;
    a sio:SIO_001121 .
}

dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance {
  dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion dcterms:description
      "[Our clinical and neurophysiological study seems to indicate that a particular condition of severe sleep disruption, similar to some extent to that reported in the fatal familial insomnia and in the Morvan fibrillary chorea, which has been indicated as Agrypnia Excitata in recent literature, might be associated with the Mulvihill-Smith syndrome.]. 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:16364148;
    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:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}