@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo> .
@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:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_head {
  this: np:hasAssertion dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_assertion;
    np:hasProvenance dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_provenance;
    np:hasPublicationInfo dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_assertion a np:Assertion .
  
  dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_provenance a np:Provenance .
  
  dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_assertion {
  miriam-gene:968 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_provenance {
  dgn-np:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_assertion dcterms:description
      "[We evaluated AQP4 expression relative to glial fibrillary acidic protein, extent of demyelination, lesion staging (CD68 staining for macrophages), and perivascular deposition of complement and immunoglobulin in 11 cases with NMO and NMO spectrum disorders (NMOSD), five with MS and 30 with other neurological diseases.]. 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:21241398;
    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:NP724443.RAZVhyiQizKjJ4vJyzVKKMKIHjR7ZA1fwQiPxPVBycLfo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}