@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk> .
@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:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_head {
  this: np:hasAssertion dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion;
    np:hasProvenance dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance;
    np:hasPublicationInfo dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion a np:Assertion .
  
  dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance a np:Provenance .
  
  dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion {
  miriam-gene:3858 a ncit:C16612 .
  
  lld:C0037277 a ncit:C7057 .
  
  dgn-gda:DGN1a0ed7a311b5142ab697256223b98492 sio:SIO_000628 miriam-gene:3858, lld:C0037277;
    a sio:SIO_001121 .
}

dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance {
  dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion dcterms:description
      "[Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic hyperkeratosis strictly confined to the palms and soles, and usually associated with mutations in the keratin K9 gene (KRT9).]. 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:15214894;
    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:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}