@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE> .
@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:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_head {
  this: np:hasAssertion dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion ;
    np:hasProvenance dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_provenance ;
    np:hasPublicationInfo dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion a np:Assertion .
  dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_provenance a np:Provenance .
  dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion {
  miriam-gene:3123 a ncit:C16612 .
  lld:C0007099 a ncit:C7057 .
  dgn-gda:DGN0d53062496d7c2fcff799d8aef02570c sio:SIO_000628 miriam-gene:3123 , lld:C0007099 ;
    a sio:SIO_001121 .
}
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_provenance {
  dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion dcterms:description "[We genotyped the human leukocyte antigens HLA-DRB1 and HLA-A, plus a panel of single nucleotide polymorphisms (SNPs) that have been associated with susceptibility to MS and then correlated the genotypes with the levels of CXCL13, as measured with ELISA in the CSF of a total of 663 patients with MS, CIS, other neurological diseases (OND) or OND with an inflammatory component (iOND).]. 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:23175382 ;
    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:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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" .
}