@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA> .
@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:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_head {
  this: np:hasAssertion dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_assertion;
    np:hasProvenance dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_provenance;
    np:hasPublicationInfo dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_assertion a np:Assertion .
  
  dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_provenance a np:Provenance .
  
  dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0302592 a ncit:C7057 .
  
  dgn-gda:DGNa74a5ec7edcd9a1cc1d724f9255ab364 sio:SIO_000628 miriam-gene:3342, lld:C0302592;
    a sio:SIO_001121 .
}

dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_provenance {
  dgn-np:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_assertion dcterms:description
      "[We applied a combination of molecular cytogenetic methods, including comparative genomic hybridization (CGH), spectral karyotyping (SKY), and fluorescence in situ hybridization (FISH), to characterize the genetic aberrations in eight widely used cervical cancer (CC) cell lines.]. 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:12557223;
    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:NP793708.RAe7CUtM9UiORgVrqJpYk2SpGV82BsB3mdnC97rxr_EEA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:07+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" .
}