@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_head {
  this: np:hasAssertion dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_assertion;
    np:hasProvenance dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_provenance;
    np:hasPublicationInfo dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_assertion a np:Assertion .
  
  dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_provenance a np:Provenance .
  
  dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_assertion {
  miriam-gene:2312 a ncit:C16612 .
  
  lld:C0011616 a ncit:C7057 .
  
  dgn-gda:DGN59bad450e9bfda3d52eef67ae0b4fc24 sio:SIO_000628 miriam-gene:2312, lld:C0011616;
    a sio:SIO_001121 .
}

dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_provenance {
  dgn-np:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_assertion dcterms:description
      "[The most important development has been the discovery that loss-of-function mutations in the gene encoding the epidermal protein filaggrin increase the risk for ICD and for nickel sensitization and nickel ACD, emphasizing the importance of the skin barrier in the pathophysiology of CD.]. 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:21329569;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP873261.RA_RWYgMmav94wSCyVGlPFH9FlX7CRWC_Sr9TM00rKsz8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:20+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}