@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_head {
  this: np:hasAssertion dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_assertion;
    np:hasProvenance dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_provenance;
    np:hasPublicationInfo dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_assertion a np:Assertion .
  
  dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_provenance a np:Provenance .
  
  dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_assertion {
  miriam-gene:1139 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN3dc2ea6778aea8647aaeb0b66e2b0b19 sio:SIO_000628 miriam-gene:1139, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_provenance {
  dgn-np:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_assertion dcterms:description
      "[In contrast to GTG banding, array CGH determined the exact number of deleted genes and thus allowed the identification of candidate genes for cleft palate (GREM1, CX36, MEIS2), congenital heart defect (ACTC, GREM1, CX36, MEIS2), and mental retardation (ARHGAP11A, CHRNA7, CHRM5).]. 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:17163532;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP314435.RAkPatsjUyyLWy0HI9bHkpLJ3_xleZyZHQZszIgFZuIHc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:40+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}