@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA> .
@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:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_head {
  this: np:hasAssertion dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_assertion;
    np:hasProvenance dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_provenance;
    np:hasPublicationInfo dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_assertion a np:Assertion .
  
  dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_provenance a np:Provenance .
  
  dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_assertion {
  miriam-gene:4599 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN9023930936982a8b4aed9b0525657745 sio:SIO_000628 miriam-gene:4599, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_provenance {
  dgn-np:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_assertion dcterms:description
      "[Exon trapping was performed from a partial cosmid, PAC, and P1 clone contig from human chromosome 21 between MX1 and 21qter to identify genes that may be involved in the pathogenesis of Down syndrome or several of the genetic diseases that map to chromosome 21q22.3.]. 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:9465297;
    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:NP683297.RAO9Bw6R5u1JpecIw6KC13KtvwTr2prbCVtHjRFxlzsYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}