@prefix semsc: <http://semanticscience.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@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 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:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_head {
   this: np:hasAssertion dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_assertion ;
    np:hasProvenance dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_provenance ;
    np:hasPublicationInfo dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_assertion a np:Assertion .
  dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_provenance a np:Provenance .
  dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_assertion {
   miriam-gene:4210 a ncit:C16612 .
  lld:C0243050 a ncit:C7057 .
  dgn-gda:DGN6ac7aa1bbb47f43122b506969fec8fbc semsc:SIO_000628 miriam-gene:4210 , lld:C0243050 ;
    a semsc:SIO_001121 .
}
dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_provenance {
   dgn-np:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_assertion dct:description "[Pericardial diseases are the most represented cardiovascular abnormalities, though the role of MEFV and TNFRSF1A in the initiation of heart involvement has not been demonstrated formally and will be discussed herein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    semsc:SIO_000772 miriam-pubmed:21284530 ;
    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:NP209466.RADIRPXeaOZy1cMh63tyAUx0blW38EXNqTQ2GtuKx9hAI130_publicationInfo {
   this: dct:created "2014-10-02T12:33:55+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject semsc:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}