@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc> .
@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:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_head {
  this: np:hasAssertion dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_assertion;
    np:hasProvenance dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_provenance;
    np:hasPublicationInfo dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_assertion a np:Assertion .
  
  dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_provenance a np:Provenance .
  
  dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_assertion {
  miriam-gene:1827 a ncit:C16612 .
  
  lld:C1860787 a ncit:C7057 .
  
  dgn-gda:DGNd1086bdc5783408d48738b27aae1a7cc sio:SIO_000628 miriam-gene:1827, lld:C1860787;
    a sio:SIO_001121 .
}

dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_provenance {
  dgn-np:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_assertion dcterms:description
      "[The Down syndrome critical region 1 (DSCR1) gene is present in the region of human chromosome 21 and the syntenic region of mouse chromosome 16, trisomy of which is associated with congenital heart defects observed in Down syndrome.]. 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:14738882;
    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:NP560155.RAqEiDG2TQLvm10zV3oANeJeh6NKEJ9V165r5ZHQqR0hc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:38+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" .
}