@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ> .
@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:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_head {
  this: np:hasAssertion dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_assertion;
    np:hasProvenance dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_provenance;
    np:hasPublicationInfo dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_assertion a np:Assertion .
  
  dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_provenance a np:Provenance .
  
  dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_assertion {
  miriam-gene:286887 a ncit:C16612 .
  
  lld:C0265334 a ncit:C7057 .
  
  dgn-gda:DGN0cbe394b5c80006c4d2bfdebd04ebecb sio:SIO_000628 miriam-gene:286887, lld:C0265334;
    a sio:SIO_001121 .
}

dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_provenance {
  dgn-np:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_assertion dcterms:description
      "[have identified KRT6C mutations in patients with focal palmoplantar keratoderma (FPPK), but debate concerning overlapping phenotypes between FPPK and pachyonychia congenita (PC) will continue because only one family has nail involvement.]. 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:20081885;
    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:NP350147.RAEQTnq_HPBxqbEUcU1aydgguJdcapnQPlUTETwWYG4pQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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" .
}