@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_head {
  this: np:hasAssertion dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_assertion;
    np:hasProvenance dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_provenance;
    np:hasPublicationInfo dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_assertion a np:Assertion .
  
  dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_provenance a np:Provenance .
  
  dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_assertion {
  miriam-gene:6239 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN2a2a5a9249594fb96b3305fc6abbb8ad sio:SIO_000628 miriam-gene:6239, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_provenance {
  dgn-np:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_assertion dcterms:description
      "[The overlapping deleted region harbors six genes (RREB1, NRN1, CAGE1, LY86, SSR1, and F13A1), of which NRN1 and RREB1 are considered as candidate genes for the intellectual disability and the overlapping dysmorphism, respectively.]. 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:23183317;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP907443.RAqNomuJnovTxtgvRWapGvkT9To7_JC9RCPPXEhx055UQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:17+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}