@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k> .
@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:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_head {
  this: np:hasAssertion dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion;
    np:hasProvenance dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance;
    np:hasPublicationInfo dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion a np:Assertion .
  
  dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance a np:Provenance .
  
  dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion {
  miriam-gene:23705 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN68ef15dfa9d8a08a8f492490eeaa3730 sio:SIO_000628 miriam-gene:23705, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance {
  dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion dcterms:description
      "[Bisulphite sequencing and genetic analysis of 18 primary neuroblastomas suggested that neither haploinsufficiency nor hypermethylation is regularly involved in CADM1 gene silencing in neuroblastoma, which is in contrast to results obtained in other malignancies.]. 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:18084322;
    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:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:04+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" .
}