@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY> .
@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:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_head {
  this: np:hasAssertion dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion;
    np:hasProvenance dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance;
    np:hasPublicationInfo dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion a np:Assertion .
  
  dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance a np:Provenance .
  
  dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0740279 a ncit:C7057 .
  
  dgn-gda:DGN4b045e6c8dd1d911199a19f679017990 sio:SIO_000628 miriam-gene:4397, lld:C0740279;
    a sio:SIO_001121 .
}

dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance {
  dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion dcterms:description
      "[The multiple sclerosis group with severe cerebellar deficit and the ADCA group both had significant cerebellar atrophy (suggesting nerve cell body and axon loss) compared with the multiple sclerosis patients with minimal or no signs of cerebellar deficit and 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:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}