@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc> .
@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:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_head {
  this: np:hasAssertion dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_assertion;
    np:hasProvenance dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_provenance;
    np:hasPublicationInfo dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_assertion a np:Assertion .
  
  dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_provenance a np:Provenance .
  
  dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_assertion {
  miriam-gene:790 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN7c022741ac8b1d2664cdfaea29eac28a sio:SIO_000628 miriam-gene:790, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_provenance {
  dgn-np:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_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:NP847839.RA7V0fWI8aX-f29HrowTjGgB5mDhGYfHjyuEXx0RknHfc130_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" .
}