@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM> .
@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/v4.0.0/void/> .

dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_head {
  this: np:hasAssertion dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_assertion;
    np:hasProvenance dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_provenance;
    np:hasPublicationInfo dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_assertion a np:Assertion .
  
  dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_provenance a np:Provenance .
  
  dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_assertion {
  miriam-gene:800 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNd0726e164fd403e689bc119c0604f3c7 sio:SIO_000628 miriam-gene:800, lld:C0010068;
    a sio:SIO_001122 .
}

dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_provenance {
  dgn-np:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_assertion dcterms:description
      "[A polymorphism in the corresponding FCG2RA gene resulting in an amino acid change (R131H) has been implicated, with conflicting results in the pathogenesis of various autoimmune or inflammatory disorders (e.g., atherosclerosis and coronary artery disease [CAD]).]. 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:20973705;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP847856.RAMcNdA_SrkYbgPYZETzXE47LSganz3VfwfBh-3oNtImM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:09+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}