@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc> .
@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:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_head {
  this: np:hasAssertion dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_assertion;
    np:hasProvenance dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_provenance;
    np:hasPublicationInfo dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_assertion a np:Assertion .
  
  dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_provenance a np:Provenance .
  
  dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_assertion {
  miriam-gene:3858 a ncit:C16612 .
  
  lld:C0022596 a ncit:C7057 .
  
  dgn-gda:DGNb2e91dd4716d2d1e4eb6ff05d9633b18 sio:SIO_000628 miriam-gene:3858, lld:C0022596;
    a sio:SIO_001121 .
}

dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_provenance {
  dgn-np:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_assertion dcterms:description
      "[Similar clumping of suprabasal keratins in bullous CIE Brocq and in palmoplantar keratoderma Voerner have been assigned to identical types of mutations in the same critical position of the rod domain in K 1, K 10, and K 9, respectively.]. 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:7525739;
    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:NP568410.RAlLBA1AFjjdC5ZD0bvBIPADE9rN0aQcjNcZVGKLvIkUc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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" .
}