@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw> .
@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:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_head {
  this: np:hasAssertion dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_assertion;
    np:hasProvenance dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_provenance;
    np:hasPublicationInfo dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_assertion a np:Assertion .
  
  dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_provenance a np:Provenance .
  
  dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0087012 a ncit:C7057 .
  
  dgn-gda:DGN932e7f283e62de8a838c30c0727339fc sio:SIO_000628 miriam-gene:2332, lld:C0087012;
    a sio:SIO_001121 .
}

dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_provenance {
  dgn-np:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_assertion dcterms:description
      "[The aim of this study was to determine the molecular basis of the disorder in patients suspected of spinocerebellar ataxias (SCAs) and search for premutation in the FMR1 gene causing FXTAS among patients in whom 9 SCA types were previously excluded.]. 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: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:NP580430.RAF7TJIDfELy55grlG6JwCJ5DSLPweDa7vaR0TVn2DFlw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:49+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" .
}