@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY> .
@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:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_head {
  this: np:hasAssertion dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion ;
    np:hasProvenance dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance ;
    np:hasPublicationInfo dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion a np:Assertion .
  dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance a np:Provenance .
  dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion {
  miriam-gene:3858 a ncit:C16612 .
  lld:C0037274 a ncit:C7057 .
  dgn-gda:DGN49546a379f6e0d7d115e3f2c32b5798f sio:SIO_000628 miriam-gene:3858 , lld:C0037274 ;
    a sio:SIO_001121 .
}
dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_provenance {
  dgn-np:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_assertion dcterms:description "[With the exciting discovery that three autosomal dominant genetic skin disorders, epidermolysis bullosa simplex (EBS), epidermolytic hyperkeratosis (EHK) and palmoplantar keratoderma (PPK), are in fact disorders of keratins comes the realization that the integrity of the keratin filament network is crucial to the structural integrity of the skin.]. 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:7528048 ;
    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:NP390586.RABzUAA_kJ5PC3aqb6etrUsv5AFuyJZt04gu6LkFIfiqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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 ;
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    pav:version "v2.1.0.0" .
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}