@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U> .
@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 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:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_head {
  this: np:hasAssertion dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_assertion;
    np:hasProvenance dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_provenance;
    np:hasPublicationInfo dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_assertion a np:Assertion .
  
  dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_provenance a np:Provenance .
  
  dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_assertion {
  miriam-gene:4713 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNfa8b4f97e45763c59abe90816b65ff45 sio:SIO_000628 miriam-gene:4713, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_provenance {
  dgn-np:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_assertion dct:description
      "[The HLA typing of 100 patients with multiple sclerosis (MS) and their differentiation according to the dynamics of the disease, the type of course and the degree of defect showed the following results: a significant increase in frequency of HLA B7 (P less than 0.05), independent of the severity of illness, a 4-fold increased frequency of the HLA haplotype A25, B18 with augmented occurrence in slight to moderate severity of the disability degree (P less than 0.05), less so in the dynamics of the disease, and only partially so in the relapsing-remittent course.]. 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:6819759;
    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:NP357365.RABDQTb_fmjC8LvAvKS4Rn6aYeOh61fUUQ4Cwq-vwYg3U130_publicationInfo {
  this: dct:created "2014-10-02T12:35:29+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}