@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0> .
@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:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_head {
  this: np:hasAssertion dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_assertion;
    np:hasProvenance dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_provenance;
    np:hasPublicationInfo dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_assertion a np:Assertion .
  
  dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_provenance a np:Provenance .
  
  dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_assertion {
  miriam-gene:2078 a ncit:C16612 .
  
  lld:C1860787 a ncit:C7057 .
  
  dgn-gda:DGNa67c54a2ddf8d94836cee66d0ab35f91 sio:SIO_000628 miriam-gene:2078, lld:C1860787;
    a sio:SIO_001121 .
}

dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_provenance {
  dgn-np:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_assertion dcterms:description
      "[We have isolated two novel genes, designated DSCR5 and DSCR6, from the Down syndrome critical region (DSCR) on chromosome 21q22.2 which has been defined as minimal overlapping region of partial trisomy 21 patients and located between t(4;21) break point and ERG (approximately 1.6 Mb).]. 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:10814524;
    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:NP316461.RAAy1D_a1tG0uOZZ_kUefNuyEQSdqW4IiKlJK1IUh24T0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}