@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes> .
@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/v4.0.0/void/> .
dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_head {
   this: np:hasAssertion dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_assertion ;
    np:hasProvenance dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_provenance ;
    np:hasPublicationInfo dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_assertion a np:Assertion .
  dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_provenance a np:Provenance .
  dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_assertion {
   miriam-gene:2678 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
  dgn-gda:DGN8443ac2f6de1a30d1efd7bf887f0e9b0 sio:SIO_000628 miriam-gene:2678 , lld:C0025362 ;
    a sio:SIO_001121 .
}
dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_provenance {
   dgn-np:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_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-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP583846.RAREUKEu3xxkOAW5gP2GQsHW5v1lpxqS8lSLavsMxfZes130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:10+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}