@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc> .
@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:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_head {
  this: np:hasAssertion dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_assertion;
    np:hasProvenance dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_provenance;
    np:hasPublicationInfo dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_assertion a np:Assertion .
  
  dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_provenance a np:Provenance .
  
  dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_assertion {
  miriam-gene:23114 a ncit:C16612 .
  
  lld:C0011303 a ncit:C7057 .
  
  dgn-gda:DGNb31d6cbc05ec6fa15f2e5367874eb745 sio:SIO_000628 miriam-gene:23114, lld:C0011303;
    a sio:SIO_001121 .
}

dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_provenance {
  dgn-np:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_assertion dcterms:description
      "[raft-association of NF155 is essential for the assembly of the paranodal junction and reduced association to lipid rafts is accompanied by the disassembly of the paranodal junction and contributes to the demyelination process in multiple sclerosis ]. 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:17405145;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP136660.RAC4VAR6lvuRtPEfGTDtmYyYNmF0UCxebVzaU9bkMy8Qc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:11+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" .
}