@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng> .
@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:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_head {
  this: np:hasAssertion dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_assertion;
    np:hasProvenance dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_provenance;
    np:hasPublicationInfo dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_assertion a np:Assertion .
  
  dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_provenance a np:Provenance .
  
  dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_assertion {
  miriam-gene:154 a ncit:C16612 .
  
  lld:C0030499 a ncit:C7057 .
  
  dgn-gda:DGNe0d117dda2e7ecb0a4e951cc97ae5aa0 sio:SIO_000628 miriam-gene:154, lld:C0030499;
    a sio:SIO_001121 .
}

dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_provenance {
  dgn-np:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_assertion dcterms:description
      "[For example, significant associations between markers in certain candidate genes (eg, STAT6, ADRB2, and IFNGR1) for traits such as high total IgE levels observed in resistance to extracellular parasitic disease in one population and atopic asthma in another supports the common disease/common variant model for disease.]. 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:16461122;
    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:NP838322.RAt4p705u2H23K37jX6Va27D2xfWmhB3lGHadzbdIHXng130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}