@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg> .
@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:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_head {
  this: np:hasAssertion dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_assertion;
    np:hasProvenance dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_provenance;
    np:hasPublicationInfo dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_assertion a np:Assertion .
  
  dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_provenance a np:Provenance .
  
  dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_assertion {
  miriam-gene:103 a ncit:C16612 .
  
  lld:C0406775 a ncit:C7057 .
  
  dgn-gda:DGN77893248aab10dee86ca32286efdeeeb sio:SIO_000628 miriam-gene:103, lld:C0406775;
    a sio:SIO_001121 .
}

dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_provenance {
  dgn-np:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_assertion dcterms:description
      "[Only three cases with neurological disorders have been reported, although more than 50 mutations of the ADAR1 gene causing DSH have been reported and none of them had any neurological symptoms.]. 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:19017046;
    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:NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}