@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE> .
@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:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_head {
  this: np:hasAssertion dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_assertion;
    np:hasProvenance dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_provenance;
    np:hasPublicationInfo dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_assertion a np:Assertion .
  
  dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_provenance a np:Provenance .
  
  dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0007760 a ncit:C7057 .
  
  dgn-gda:DGN798a0f7bff9847bb58d531831163ab96 sio:SIO_000628 miriam-gene:4397, lld:C0007760;
    a sio:SIO_001121 .
}

dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_provenance {
  dgn-np:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_assertion dcterms:description
      "[Proton magnetic resonance spectroscopy (MRS) and MRI were carried out in 11 patients with multiple sclerosis who had clinical evidence of severe cerebellar involvement, 11 multiple sclerosis patients (of similar age and disease duration) who had minimal or no signs of cerebellar disease, eight patients with autosomal dominant cerebellar ataxia (ADCA) and 11 healthy 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:8595487;
    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:NP665155.RAYs4aewzGW3uoe_e6v__5nZK_n6x7BlXCBUbnkEDcbcE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:42+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" .
}