@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700> .
@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:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_head {
  this: np:hasAssertion dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_assertion;
    np:hasProvenance dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_provenance;
    np:hasPublicationInfo dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_assertion a np:Assertion .
  
  dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_provenance a np:Provenance .
  
  dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_assertion {
  miriam-gene:23405 a ncit:C16612 .
  
  lld:C1297882 a ncit:C7057 .
  
  dgn-gda:DGN0a899f7efd8d724473ef7da971e7ad10 sio:SIO_000628 miriam-gene:23405, lld:C1297882;
    a sio:SIO_001121 .
}

dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_provenance {
  dgn-np:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_assertion dcterms:description
      "[Observations of patients with partial trisomy of the 21q22.2 fragment suggest that most of the signs of the syndrome, including mental retardation, could be influenced by the region referred to as the Down Minimal Chromosomal Region-1 (DCR-1) for that reason.]. 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:15520513;
    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:NP861781.RAnr1FmxMwEPlDM1dMTSOVDkhhO3GEJ7vIPTCfx1Dk700130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}