@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o> .
@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:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_head {
  this: np:hasAssertion dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion;
    np:hasProvenance dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance;
    np:hasPublicationInfo dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion a np:Assertion .
  
  dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance a np:Provenance .
  
  dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0242621 a ncit:C7057 .
  
  dgn-gda:DGN2bd6f5767279ac4d8c7d6420c514aab9 sio:SIO_000628 miriam-gene:3342, lld:C0242621;
    a sio:SIO_001121 .
}

dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance {
  dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion dcterms:description
      "[Comparative genomic hybridization (CGH) revealed regions of gains and amplification in three locations, with gains of chromosome 7, amplification of 8q24 (corresponding to the MYCC locus) and gains of the long arm of chromosome 17 (suggestive of isochromosome 17q).]. 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:10643003;
    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:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}