@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE> .
@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:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_head {
  this: np:hasAssertion dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_assertion ;
    np:hasProvenance dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_provenance ;
    np:hasPublicationInfo dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_assertion a np:Assertion .
  dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_provenance a np:Provenance .
  dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  lld:C0345905 a ncit:C7057 .
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}
dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_provenance {
  dgn-np:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_assertion dcterms:description "[It is concluded that the combination of lamin ICC and FISH improves chromosome copy number analysis and can be used to investigate genomic changes in different tumor compartments in thin frozen tissue sections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP521929.RAHtpn_brv21U5t_HNK1BO3_wdblkvicnmYVjpyeRb2HE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    prv:usedData dgn-void:disgenetrdf ;
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}