@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA> .
@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:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_head {
  this: np:hasAssertion dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_assertion ;
    np:hasProvenance dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_provenance ;
    np:hasPublicationInfo dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_assertion a np:Assertion .
  dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_provenance a np:Provenance .
  dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_assertion {
  miriam-gene:11240 a ncit:C16612 .
  lld:C0014072 a ncit:C7057 .
  dgn-gda:DGNa6894d69d589510c4a3213fe8ab428cf sio:SIO_000628 miriam-gene:11240 , lld:C0014072 ;
    a sio:SIO_001121 .
}
dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_provenance {
  dgn-np:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_assertion dcterms:description "[Even though the PAD2 knockout mice displayed a dramatic reduction in the amount of citrullination present in the CNS, indicating that PAD2 is indeed responsible for the majority of detectable citrullination observed in EAE, the development of EAE was not impaired by genetic deletion of PAD2, suggesting that PAD2 catalyzed citrullination is not essential to the development of EAE.]. 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:16856138 ;
    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:NP161739.RA93bXYL-wXcOaKMV-aWIMQe09gY0kNlkGkPMXCXm8VOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}