@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys> .
@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:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_head {
  this: np:hasAssertion dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_assertion;
    np:hasProvenance dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_provenance;
    np:hasPublicationInfo dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_assertion a np:Assertion .
  
  dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_provenance a np:Provenance .
  
  dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_assertion {
  miriam-gene:26683 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN4d26f7933e7ec391b4ed4bdb92174316 sio:SIO_000628 miriam-gene:26683, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_provenance {
  dgn-np:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_assertion dcterms:description
      "[Polymorphisms producing small but statistically significant increases in asthma risk (OR 1.1 per allele) were identified in DPP10 and ADAM33, with the strongest evidence being for SNPs tagging the DPP10 gene.]. 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:19237393;
    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:NP579993.RAQfNCynSuMjSsPcf3PsY3PbcdVUQXrsPpcBArYx_N4ys130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:49+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" .
}