@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM> .
@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 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:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_head {
  this: np:hasAssertion dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_assertion;
    np:hasProvenance dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_provenance;
    np:hasPublicationInfo dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_assertion a np:Assertion .
  
  dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_provenance a np:Provenance .
  
  dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_assertion {
  miriam-gene:868 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN696b897ec2ee24306c91a6639363568a sio:SIO_000628 miriam-gene:868, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_provenance {
  dgn-np:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_assertion dct:description
      "[Although differences between individual families can only be suggested, the aggregate results in multiplex families demonstrate effect sizes that are increased as compared with those reported in previous studies for sporadic cases.]. 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:19506219;
    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:NP79123.RA9NljFP8ntKDzhXx1l3koCUPpVpAiymFqNddBPsUNGeM130_publicationInfo {
  this: dct:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}