@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ> .
@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:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_head {
  this: np:hasAssertion dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_assertion;
    np:hasProvenance dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_provenance;
    np:hasPublicationInfo dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_assertion a np:Assertion .
  
  dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_provenance a np:Provenance .
  
  dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_assertion {
  miriam-gene:6670 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNc69e233b9553a3c82ce5fb08aa262e87 sio:SIO_000628 miriam-gene:6670, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_provenance {
  dgn-np:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_assertion dcterms:description
      "[To evaluate differential gene expression in multiple sclerosis (MS) patients and control subjects, we used differential display to screen for messenger RNAs that are differentially expressed in peripheral blood mononuclear cells from monozygotic twins who are discordant for MS. We identified a 232-bp complementary DNA fragment, present only in material from the normal twin, that exhibited 100% identity with the inhibitory transcription factor Sp3.]. 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:8687178;
    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:NP862039.RAWhiapV_iDjFWeth2R5GEIeMJZJDXc4C9TY0_QLOl5bQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}