@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU> .
@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:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_head {
  this: np:hasAssertion dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_assertion;
    np:hasProvenance dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_provenance;
    np:hasPublicationInfo dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_assertion a np:Assertion .
  
  dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_provenance a np:Provenance .
  
  dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_assertion {
  miriam-gene:80896 a ncit:C16612 .
  
  lld:C1839839 a ncit:C7057 .
  
  dgn-gda:DGN25f81173701cc0ed51d394cc0e8a3f03 sio:SIO_000628 miriam-gene:80896, lld:C1839839;
    a sio:SIO_001121 .
}

dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_provenance {
  dgn-np:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_assertion dcterms:description
      "[Although the heterogeneity analysis produced less impressive results (highest NPL score of 3.32) and a less consistent picture, we achieved evidence of locus heterogeneity at chromosomes 2q, 6p, 11p, 13q, and 22q, which was supported by adjacent markers within each region and by previously reported BPAD linkage findings.]. 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:17924339;
    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:NP876520.RAtu2RJQxFbTaa4S-Uk1VfpL9BDBdrPzNRa-9QI-H9LSU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}