@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8> .
@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:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_head {
  this: np:hasAssertion dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_assertion;
    np:hasProvenance dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_provenance;
    np:hasPublicationInfo dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_assertion a np:Assertion .
  
  dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_provenance a np:Provenance .
  
  dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_assertion {
  miriam-gene:4700 a ncit:C16612 .
  
  lld:C2931161 a ncit:C7057 .
  
  dgn-gda:DGNe308a63e0727c08fdbcf100f19a9d0ca sio:SIO_000628 miriam-gene:4700, lld:C2931161;
    a sio:SIO_001121 .
}

dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_provenance {
  dgn-np:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_assertion dcterms:description
      "[No significant association was found with the former polymorphisms and the observed associations with TNFa2 allele and haplotypes TNFa2b1 and TNFa2b3 were proven to be secondary to their occurrence on the B14-DR1 and B8-DR3 haplotypes, previously reported to be associated with susceptibility to IgAD.]. 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:10852388;
    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:NP360275.RAS2_pCtGgybC8axZHlV-MgGdPds030dywsMfVsXXVXJ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}