@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34> .
@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:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_head {
  this: np:hasAssertion dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_assertion;
    np:hasProvenance dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_provenance;
    np:hasPublicationInfo dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_assertion a np:Assertion .
  
  dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_provenance a np:Provenance .
  
  dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0027962 a ncit:C7057 .
  
  dgn-gda:DGNb9f4916e62e9b578daa4419a855058f2 sio:SIO_000628 miriam-gene:595, lld:C0027962;
    a sio:SIO_001121 .
}

dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_provenance {
  dgn-np:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_assertion dcterms:description
      "[We evaluated a fluorescence in situ hybridization (FISH) assay, which has previously been shown to be of value for the diagnosis of melanocytic nevi and melanomas of the skin, using probes targeting 6p25 (RREB1), 6q23 (MYB), 11q13 (CCND1) and centromere 6 (CEP6), for its potential to assist in the distinction of conjunctival melanocytic nevi from melanomas.]. 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:20100177;
    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:NP609593.RAA9lle9siK1LF--HyLINw85hZH9kr7cszt0mnYfzvq34130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:06+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" .
}