@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE> .
@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:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_head {
   this: np:hasAssertion dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_assertion ;
    np:hasProvenance dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_provenance ;
    np:hasPublicationInfo dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_assertion a np:Assertion .
  dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_provenance a np:Provenance .
  dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_assertion {
   miriam-gene:89832 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
  dgn-gda:DGN09d02fabb948d3390b08dcf193bd4a8e sio:SIO_000628 miriam-gene:89832 , lld:C0025362 ;
    a sio:SIO_001121 .
}
dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_provenance {
   dgn-np:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_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:NP583847.RA-K1ZiKxedxYRAiIUy7FM6N1ENZbJ4UntcB_V1_NrUaE130_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" .
}