@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME> .
@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:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_head {
  this: np:hasAssertion dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_assertion;
    np:hasProvenance dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_provenance;
    np:hasPublicationInfo dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_assertion a np:Assertion .
  
  dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_provenance a np:Provenance .
  
  dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_assertion {
  miriam-gene:2209 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN5388ba88938ccf6ac1e810d90912198b sio:SIO_000628 miriam-gene:2209, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_provenance {
  dgn-np:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_assertion dcterms:description
      "[Unlike other genetic polymorphisms reported in periodontology, most Fcγ receptor polymorphisms reported not only have established biological functions but are reported to associate with other autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus.]. 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:22117888;
    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:NP468419.RA-MFAEPejgwHhRPdlg9LeErO68g4EsYDZd3Pg_11ScME130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+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" .
}