@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_head {
  this: np:hasAssertion dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_assertion ;
    np:hasProvenance dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_provenance ;
    np:hasPublicationInfo dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_assertion a np:Assertion .
  dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_provenance a np:Provenance .
  dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  lld:C0031069 a ncit:C7057 .
  dgn-gda:DGNa7a1a45a0f1e06cf85728f448f6f2eea sio:SIO_000628 miriam-gene:4210 , lld:C0031069 ;
    a sio:SIO_001122 .
}
dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_provenance {
  dgn-np:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_assertion dcterms:description "[We found an increased frequency of MEFV variants in AS patients as compared with healthy controls and with RA patient controls. This was primarily due to the presence of M694V. The roles of other exon 10 variants, as well as the relationship between the v]. 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:20533539 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP68815.RA-rMXoe3KUR1l1NF0zs0P9SsvroI2ajX58RWOEW0J2fo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:17+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}