@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848> .
@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:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_head {
  this: np:hasAssertion dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion;
    np:hasProvenance dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_provenance;
    np:hasPublicationInfo dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion a np:Assertion .
  
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  dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C1621958 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_provenance {
  dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion dcterms:description
      "[The present study compares the CGH evaluation of 22 GBM with classic cytogenetics, loss of heterozygosity by allelotyping, and gene amplification by Southern blot analysis to determine the reliability of CGH in the genetic characterization of GBM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:39+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>,
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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