@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA> .
@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:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_head {
  this: np:hasAssertion dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion;
    np:hasProvenance dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance;
    np:hasPublicationInfo dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion a np:Assertion .
  
  dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance a np:Provenance .
  
  dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C0029134 a ncit:C7057 .
  
  dgn-gda:DGN7b683a671c05249df58acac994e00928 sio:SIO_000628 miriam-gene:3918, lld:C0029134;
    a sio:SIO_001121 .
}

dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance {
  dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion dcterms:description
      "[The cerebrospinal fluid (CSF) and serum from 64 patients with multiple sclerosis (MS) and 47 patients with monosymptomatic optic neuritis (ON) were analyzed for the distribution of allotypic determinants on IgG and compared to similar samples from 51 patients with other neurological diseases (OND) as well as to serum samples from 97 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:6713741;
    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:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}