@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8> .
@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/v3.0.0/void/> .

dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_head {
  this: np:hasAssertion dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_assertion;
    np:hasProvenance dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_provenance;
    np:hasPublicationInfo dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_assertion a np:Assertion .
  
  dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_provenance a np:Provenance .
  
  dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_assertion {
  miriam-gene:2334 a ncit:C16612 .
  
  lld:C0424605 a ncit:C7057 .
  
  dgn-gda:DGNd6d6f5d07aeaafcae51b68aac0b090a2 sio:SIO_000628 miriam-gene:2334, lld:C0424605;
    a sio:SIO_001121 .
}

dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_provenance {
  dgn-np:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_assertion dcterms:description
      "[To see whether FRAXA or FRAXE can account for the etiology of some unexplained neurodevelopmental disorders in children, we screened for trinucleotide repeat expansion in a consecutive cohort of 73 Chinese children and their mothers seen in 1995 (group 1) referred for developmental assessment due to developmental delay, language delay, attention deficit hyperactivity disorder, autistic spectrum disorder, mental retardation and/or learning disability.]. 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:9630071;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP409223.RA9dyXIWWJT20C7QWxZtCZO9iXQKi6ImXMtwVDw4cu0j8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:38+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}