@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE> .
@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:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_head {
  this: np:hasAssertion dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion;
    np:hasProvenance dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance;
    np:hasPublicationInfo dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion a np:Assertion .
  
  dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance a np:Provenance .
  
  dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN06c5b4e99cdfa4c0785d3773d5588397 sio:SIO_000628 miriam-gene:3342, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance {
  dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion dcterms:description
      "[The molecular cytogenetic techniques of fluorescent in situ hybridization (FISH), comparative genomic hybridization (CGH), and spectral karyotyping (SKY) are providing tremendous insights into genetic information related to cancer by specifically illustrating chromosomal abnormalities that can occur in a patient's cancer cells.]. 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:11899766;
    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:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}