@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c> .
@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:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_head {
  this: np:hasAssertion dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion;
    np:hasProvenance dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance;
    np:hasPublicationInfo dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion a np:Assertion .
  
  dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance a np:Provenance .
  
  dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion {
  miriam-gene:80381 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN655c75304d878585e51b6373080d3e57 sio:SIO_000628 miriam-gene:80381, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance {
  dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion dcterms:description
      "[A whole genome association scan suggested that allelic variants in the CD58 gene region, encoding the costimulatory molecule LFA-3, are associated with risk of developing MS. We now report additional genetic evidence, as well as resequencing and fine mapping of the CD58 locus in patients with MS and control subjects.]. 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:19237575;
    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:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}