@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA> .
@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:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_head {
  this: np:hasAssertion dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion ;
    np:hasProvenance dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance ;
    np:hasPublicationInfo dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion a np:Assertion .
  dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance a np:Provenance .
  dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion {
  miriam-gene:100288695 a ncit:C16612 .
  lld:C0041107 a ncit:C7057 .
  dgn-gda:DGN2e19d8d8313f48a59d5f16c230a03af4 sio:SIO_000628 miriam-gene:100288695 , lld:C0041107 ;
    a sio:SIO_001121 .
}
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance {
  dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion dcterms:description "[The present study suggested that deletion of evolutionarily conserved developmental genes (RGPD5, RGPD and LIMS3) in the 2q13 region might have contributed to more severity in phenotype as compared to so far such reported cases of 18p trisomy's, as these are involved in nuclear-cytoplasm trafficking, signaling for tissue patterning and differentiation.]. 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:25617521 ;
    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:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:16+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" .
}