@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A> .
@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:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_head {
  this: np:hasAssertion dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_assertion;
    np:hasProvenance dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_provenance;
    np:hasPublicationInfo dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_assertion a np:Assertion .
  
  dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_provenance a np:Provenance .
  
  dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C0027819 a ncit:C7057 .
  
  dgn-gda:DGNfcd87076a1559e02d0a238980e3e5618 sio:SIO_000628 miriam-gene:8718, lld:C0027819;
    a sio:SIO_001121 .
}

dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_provenance {
  dgn-np:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_assertion dcterms:description
      "[Among the best candidate genes predisposing to the development of neuroblastoma located in 1p36, the AJAP1 gene is the only gene present in the duplication while CHD5, TNFRSF25 and CAMTA1 are located outside of the rearrangement.]. 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:18672103;
    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:NP160513.RAd3ufZ4Qg1L9zBF8L2SToHzknbTxAoFnmmdBf0k56u2A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}