@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU> .
@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:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_head {
  this: np:hasAssertion dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_assertion;
    np:hasProvenance dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_provenance;
    np:hasPublicationInfo dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_assertion a np:Assertion .
  
  dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_provenance a np:Provenance .
  
  dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_assertion {
  miriam-gene:3852 a ncit:C16612 .
  
  lld:C0037274 a ncit:C7057 .
  
  dgn-gda:DGN4657af61857d072ef878dbb0ffb8d067 sio:SIO_000628 miriam-gene:3852, lld:C0037274;
    a sio:SIO_001121 .
}

dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_provenance {
  dgn-np:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_assertion dcterms:description
      "[Epidermolysis bullosa simplex (EBS) is an inherited skin disorder caused by mutations in keratins K5 (keratin 5) and K14 (keratin 14), with fragility of basal keratinocytes leading to epidermal cytolysis and blistering.]. 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:17039244;
    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:NP474303.RA-dCuBblxJAuWCFkoFkeCgdclZM86w-lyDMk-terdorU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:44+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" .
}