@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k> .
@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:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_head {
  this: np:hasAssertion dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_assertion;
    np:hasProvenance dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_provenance;
    np:hasPublicationInfo dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_assertion a np:Assertion .
  
  dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_provenance a np:Provenance .
  
  dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_assertion {
  miriam-gene:81704 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNedd337abe9a34cd9bc53ff33cb8ce013 sio:SIO_000628 miriam-gene:81704, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_provenance {
  dgn-np:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_assertion dcterms:description
      "[However, unanswered questions remain regarding how the absence of DOCK8 also leads to high IgE and allergic disease, predisposition for malignancy, and unusual clinical features, such as CNS abnormalities and autoimmunity, observed in some patients.]. 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:22236427;
    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:NP213157.RAgoaflFu1q_lAfkm_A-h11QBKqlouEOtkXg6RiyOG5_k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}