@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I> .
@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:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_head {
  this: np:hasAssertion dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_assertion;
    np:hasProvenance dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_provenance;
    np:hasPublicationInfo dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_assertion a np:Assertion .
  
  dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_provenance a np:Provenance .
  
  dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_assertion {
  miriam-gene:84650 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN0aee6429142ccd6a287746aba640e641 sio:SIO_000628 miriam-gene:84650, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_provenance {
  dgn-np:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_assertion dcterms:description
      "[The neuropsychological testing and ERP results of the present study provide support for the hypothesis that executive dysfunction is the primary cognitive impairment among older female premutation carriers both with and without FXTAS, although these deficits are relatively mild compared to those in FXTAS males.]. 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:23686745;
    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:NP1078830.RA7unf_LtZKq5HCbWoiYtk6spP-wn5S4oJIjwWjnxms8I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:55+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}