@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec> .
@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:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_head {
  this: np:hasAssertion dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_assertion;
    np:hasProvenance dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_provenance;
    np:hasPublicationInfo dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_assertion a np:Assertion .
  
  dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_provenance a np:Provenance .
  
  dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_assertion {
  miriam-gene:7321 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN732bda0192047c3ebdab3043dc415b84 sio:SIO_000628 miriam-gene:7321, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_provenance {
  dgn-np:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_assertion dcterms:description
      "[In these patients, the electroclinical pattern of theta waves (probably unrelated to epilepsy) and the SW and SFT, even with mild mental retardation (MR) or no MR and without dysmorphic features, suggest that the r(20) syndrome may be present.]. 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:9738673;
    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:NP702899.RA8MDzjPFaZP2xZ2e4cWS0UPSawnNfwo4zo3eboX-DPec130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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" .
}