@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o> .
@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:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_head {
  this: np:hasAssertion dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_assertion;
    np:hasProvenance dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_provenance;
    np:hasPublicationInfo dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_assertion a np:Assertion .
  
  dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_provenance a np:Provenance .
  
  dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN6bcc89e311bdb59154b1e98c0c383c6f sio:SIO_000628 miriam-gene:3265, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_provenance {
  dgn-np:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_assertion dcterms:description
      "[These `giant` spindles were not associated with any evidence of structural damage of the cortex or the thalami and should be considered as phenotypic feature of sleep EEG activity in Costello syndrome because of HRAS mutation.]. 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:21633259;
    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:NP401361.RAdTNxY9fbrTUUp71Mve51oElg6N86ByQyZaKUQDv121o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:59+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" .
}