@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0> .
@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:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_head {
   this: np:hasAssertion dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_assertion ;
    np:hasProvenance dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_provenance ;
    np:hasPublicationInfo dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_assertion a np:Assertion .
  dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_provenance a np:Provenance .
  dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_assertion {
   miriam-gene:2312 a ncit:C16612 .
  lld:C0017638 a ncit:C7057 .
  dgn-gda:DGNca2e062a9faebba9997be7097847952e sio:SIO_000628 miriam-gene:2312 , lld:C0017638 ;
    a sio:SIO_001121 .
}
dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_provenance {
   dgn-np:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_assertion dcterms:description "[Areas of progress include valid and repeatable methods of disease definition, global documentation of disease prevalence and impact, clarification of the role of some genetic factors, such as filaggrin gene mutations, clear evidence that environmental factors are key, as demonstrated by the positive social class gradient and rising prevalence, a possible protective effect of infections in early life, documentation of comorbidities, such as a reduced risk of glioma, and mapping the evidence base through systematic reviews and an online global resource of clinical trials.]. 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:23331673 ;
    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:NP896821.RAAiDb3CpS1_UtGnAp7UxBl9LrI7Qx046dm3cnHrZ93l0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:11+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" .
}