@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ> .
@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:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_head {
  this: np:hasAssertion dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_assertion;
    np:hasProvenance dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_provenance;
    np:hasPublicationInfo dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_assertion a np:Assertion .
  
  dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_provenance a np:Provenance .
  
  dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_assertion {
  miriam-gene:3627 a ncit:C16612 .
  
  lld:C0242656 a ncit:C7057 .
  
  dgn-gda:DGN9aa8798506e8424da323cfe40ae30515 sio:SIO_000628 miriam-gene:3627, lld:C0242656;
    a sio:SIO_001122 .
}

dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_provenance {
  dgn-np:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_assertion dcterms:description
      "[GGTT haplotype of CXCL10 gene is not susceptibility factor for development of multiple sclerosis (MS), but is probably to influence the course of MS, possibly contributing to slow down disease progression.]. 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:17250724;
    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:NP141325.RAwSPhZQthD1LGxhRLMBd2-tJZMrCCsJEBE59B6fbbkrQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:14+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" .
}