@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k> .
@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:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_head {
  this: np:hasAssertion dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_assertion;
    np:hasProvenance dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_provenance;
    np:hasPublicationInfo dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_assertion a np:Assertion .
  
  dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_provenance a np:Provenance .
  
  dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_assertion {
  miriam-gene:3858 a ncit:C16612 .
  
  lld:C0079298 a ncit:C7057 .
  
  dgn-gda:DGN504823dd0b1447e9287628afaa7846cc sio:SIO_000628 miriam-gene:3858, lld:C0079298;
    a sio:SIO_001121 .
}

dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_provenance {
  dgn-np:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_assertion dcterms:description
      "[Whereas mosaic forms have been reported for EHK, which is caused by mutations in the suprabasal keratins K1 or K10, this has never been reported for EBS, which is due to mutations in the basal keratins K5 or K14.]. 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:15388990;
    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:NP616730.RAYRpwCO-d6zSps8rkqRhdr9q2kDYkdobuvrawUb7Rd0k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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" .
}