@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ> .
@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:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_head {
  this: np:hasAssertion dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_assertion;
    np:hasProvenance dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_provenance;
    np:hasPublicationInfo dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_assertion a np:Assertion .
  
  dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_provenance a np:Provenance .
  
  dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_assertion {
  miriam-gene:2395 a ncit:C16612 .
  
  lld:C0013362 a ncit:C7057 .
  
  dgn-gda:DGN0788a7e0440e039d37294b3468548f00 sio:SIO_000628 miriam-gene:2395, lld:C0013362;
    a sio:SIO_001121 .
}

dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_provenance {
  dgn-np:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_assertion dcterms:description
      "[FXN RNA and protein levels are reduced in patients leading to progressive gait and limb ataxia, sensory loss, reduced tendon reflexes, dysarthria, absent lower limb reflexes, and loss of position and vibration sense.]. 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:22764244;
    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:NP874575.RAzlQeUAaq-5B23pyBl8QyUWSrp6zOWZtUNgwfK2IB1FQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}