@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA> .
@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:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_head {
  this: np:hasAssertion dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion ;
    np:hasProvenance dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance ;
    np:hasPublicationInfo dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion a np:Assertion .
  dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance a np:Provenance .
  dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion {
  miriam-gene:3858 a ncit:C16612 .
  lld:C0037274 a ncit:C7057 .
  dgn-gda:DGNec93df8c5b855e87f26f368f48d14370 sio:SIO_000628 miriam-gene:3858 , lld:C0037274 ;
    a sio:SIO_001121 .
}
dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_provenance {
  dgn-np:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_assertion dcterms:description "[Analyzing keratin gene sequences, appreciating the switch in keratin gene expression that takes place as epidermal cells commit to terminally differentiate, and elucidating how keratins assemble into 10 nm filaments, have provided the foundation that has led to the discoveries of the genetic bases of two major classes of human skin diseases, epidermolysis bullosa simplex (EBS) and epidermolytic hyperkeratosis (EH).]. 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:7520042 ;
    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:NP491620.RAst3QR7oQglMIeHwz4HV6oVXHyg4xYJOeKxKKK2XNngA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}