@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA> .
@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:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_head {
  this: np:hasAssertion dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_assertion ;
    np:hasProvenance dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_provenance ;
    np:hasPublicationInfo dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_provenance a np:Provenance .
  dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_assertion {
  miriam-gene:3868 a ncit:C16612 .
  lld:C0870082 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_provenance {
  dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_assertion dcterms:description "[Here, we report that overexpression of a wild-type human K16 gene in a tissue-specific fashion in transgenic mice causes aberrant keratinization of the hair follicle outer root sheath and proximal epidermis, and it leads to hyperproliferation and increased thickness of the living layers (acanthosis), as well as cornified layers (hyperkeratosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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  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 .
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dgn-np:NP306349.RAON13EZJjlOXqaAdMEA1EUAunB1llSnXDIJG5LZX1hCA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+02:00"^^xsd:dateTime ;
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