@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ> .
@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:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_head {
  this: np:hasAssertion dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_assertion;
    np:hasProvenance dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_provenance;
    np:hasPublicationInfo dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_assertion a np:Assertion .
  
  dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_provenance a np:Provenance .
  
  dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0087012 a ncit:C7057 .
  
  dgn-gda:DGNce51f3a1b42c65fcc3f34279d198f4b9 sio:SIO_000628 miriam-gene:1822, lld:C0087012;
    a sio:SIO_001122 .
}

dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_provenance {
  dgn-np:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_assertion dcterms:description
      "[The low frequency of FXTAS in the studied material probably results from the fact that the syndrome is much more common in elderly persons (penetrance of the pathogenic premutation gene is higher among elderly individuals).]. 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:19235102;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP54143.RAY_D4PiSfuMNFnKNuz2ucVpNPsdoxWBJdPgo3Gs5GlyQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:09+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" .
}