@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c> .
@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:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_head {
  this: np:hasAssertion dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_assertion;
    np:hasProvenance dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_provenance;
    np:hasPublicationInfo dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_assertion a np:Assertion .
  
  dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_provenance a np:Provenance .
  
  dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_assertion {
  miriam-gene:7051 a ncit:C16612 .
  
  lld:C0037277 a ncit:C7057 .
  
  dgn-gda:DGN7d2593ce511a0b9c2f3aca82475a59bf sio:SIO_000628 miriam-gene:7051, lld:C0037277;
    a sio:SIO_001121 .
}

dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_provenance {
  dgn-np:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_assertion dcterms:description
      "[The recent identification of genetic skin diseases with mutations in the genes encoding some of these proteins, including transglutaminase 1 and loricrin, has disclosed that abnormal cornified cell envelope synthesis is significantly involved in the pathophysiology of certain inherited keratodermas and reflects perturbations in the complex, yet highly orderly process of cornified cell envelope formation in normal skin biology.]. 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:9517915;
    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:NP557587.RAUnDCH9RAs_RKvZfVOvff8VjdCAnijvdSJLTGoQusz4c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:36+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" .
}