@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug> .
@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:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_head {
  this: np:hasAssertion dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion;
    np:hasProvenance dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance;
    np:hasPublicationInfo dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion a np:Assertion .
  
  dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance a np:Provenance .
  
  dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion {
  miriam-gene:2215 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN2814294c08345d2153f503e0da5ea799 sio:SIO_000628 miriam-gene:2215, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance {
  dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion dcterms:description
      "[Given the genetic overlap between systemic lupus erythematosus and systemic sclerosis (SSc) and the strong evidence for FCGR3B CN in the pathology of SLE, we hypothesised that FCGR3B gene dosage influences susceptibility to SSc.]. 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:22551723;
    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:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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" .
}