@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4> .
@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:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_head {
  this: np:hasAssertion dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_assertion;
    np:hasProvenance dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_provenance;
    np:hasPublicationInfo dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_assertion a np:Assertion .
  
  dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_provenance a np:Provenance .
  
  dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_assertion {
  miriam-gene:127534 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNaa9780dca9a067c0cc321ebde1d22fd3 sio:SIO_000628 miriam-gene:127534, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_provenance {
  dgn-np:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_assertion dcterms:description
      "[There is now a considerable overlap with other gap junction disorders and we propose that some cases of erythrokeratodermia variabilis without mutations in either GJB3 or GJB4 but with deafness may be caused by mutations in GJB2.]. 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:16280295;
    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:NP324626.RAJ9gX57wqfu5DKmLWGhU92Ka-XO7i7eerOQwMy5O7Jq4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}