@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0> .
@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:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_head {
  this: np:hasAssertion dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_assertion;
    np:hasProvenance dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_provenance;
    np:hasPublicationInfo dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_assertion a np:Assertion .
  
  dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_provenance a np:Provenance .
  
  dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C1839780 a ncit:C7057 .
  
  dgn-gda:DGNb17b4348a61d0582037d8673e4d29ccf sio:SIO_000628 miriam-gene:2477, lld:C1839780;
    a sio:SIO_001121 .
}

dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_provenance {
  dgn-np:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_assertion dcterms:description
      "[Using the CATSYS system to quantify movement abnormalities, we were able to record tremor, postural sway, manual (hand and finger) coordination, and reaction time in males with the FMR1 premutation, both with and without FXTAS, and compare them to controls.]. 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:18241072;
    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:NP231922.RAz7RgVSyibXmvCRnHxvDZ3zk_ojSmBohDiqDnjdTv8o0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}