@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg> .
@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:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_head {
  this: np:hasAssertion dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion;
    np:hasProvenance dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance;
    np:hasPublicationInfo dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion a np:Assertion .
  
  dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance a np:Provenance .
  
  dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion {
  miriam-gene:129563 a ncit:C16612 .
  
  lld:C0796113 a ncit:C7057 .
  
  dgn-gda:DGNc6dd6b962964723a261d1b354c594320 sio:SIO_000628 miriam-gene:129563, lld:C0796113;
    a sio:SIO_001121 .
}

dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance {
  dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion dcterms:description
      "[It has been postulated that the clinical features of Perlman syndrome result from disordered RNA metabolism and, though the precise targets of DIS3L2 have yet to be characterized, in cellular models DIS3L2 knockdown is associated with abnormalities of cell growth and division.]. 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:23613427;
    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:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:52+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" .
}