@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ> .
@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:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_head {
  this: np:hasAssertion dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_assertion;
    np:hasProvenance dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_provenance;
    np:hasPublicationInfo dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_assertion a np:Assertion .
  
  dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_provenance a np:Provenance .
  
  dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_assertion {
  miriam-gene:911 a ncit:C16612 .
  
  lld:C0043324 a ncit:C7057 .
  
  dgn-gda:DGNbfea8ae77704f6327a9b159e0a9ef80f sio:SIO_000628 miriam-gene:911, lld:C0043324;
    a sio:SIO_001121 .
}

dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_provenance {
  dgn-np:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_assertion dcterms:description
      "[From these data it is suggested that the cells involved are of indeterminate dermal histiocyte lineage and that occurrence of deep located lesions of JXG may be due to migration of CD1 a-positive histiocytes.]. 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:1379572;
    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:NP387456.RAOPXe_Uu6CSRWtQ6l8zCJfGAgIPqBYGHylnmO9dwhtnQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:50+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" .
}