@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E> .
@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:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_head {
  this: np:hasAssertion dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_assertion;
    np:hasProvenance dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_provenance;
    np:hasPublicationInfo dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_assertion a np:Assertion .
  
  dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_provenance a np:Provenance .
  
  dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_assertion {
  miriam-gene:1836 a ncit:C16612 .
  
  lld:C1850554 a ncit:C7057 .
  
  dgn-gda:DGNfb55ed12ebec01afbcb5e32e19fdf200 sio:SIO_000628 miriam-gene:1836, lld:C1850554;
    a sio:SIO_001121 .
}

dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_provenance {
  dgn-np:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_assertion dcterms:description
      "[It was suggested that DLCD might be part of the SLC26A2 spectrum of phenotypes, both because of the Finnish origin of the original family and of radiographic similarities to ACG1B and AO2.]. 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:18708426;
    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:NP169231.RARNDeJYoLmJNjEVvGYc41QR4RPw5XTrgB16D-FlQ-P5E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}