@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic> .
@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:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_head {
  this: np:hasAssertion dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_assertion;
    np:hasProvenance dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_provenance;
    np:hasPublicationInfo dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_assertion a np:Assertion .
  
  dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_provenance a np:Provenance .
  
  dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_assertion {
  miriam-gene:3565 a ncit:C16612 .
  
  lld:C0019069 a ncit:C7057 .
  
  dgn-gda:DGNcb3bab322912c0491d4b30e572178321 sio:SIO_000628 miriam-gene:3565, lld:C0019069;
    a sio:SIO_001121 .
}

dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_provenance {
  dgn-np:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_assertion dcterms:description
      "[Factor VIII gene mutations and genetic polymorphisms of the IL1beta, IL4, and IL10 genes, known to influence antibody production in autoimmune diseases, were analyzed in 164 patients (124 with severe, 26 with moderate, and 14 with mild disease) in 78 unrelated families with hemophilia A. Seventy-seven (47%) patients in 54 families had a history of inhibitors (57 high responding, 20 low responding).]. 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:16380445;
    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:NP503730.RAORS8T7B2XP4ThmLSbdY_i2QI1V0qNn34gruq9G_S4ic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}