@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw> .
@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:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_head {
   this: np:hasAssertion dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_assertion ;
    np:hasProvenance dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_provenance ;
    np:hasPublicationInfo dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_assertion a np:Assertion .
  dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_provenance a np:Provenance .
  dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_assertion {
   miriam-gene:2312 a ncit:C16612 .
  lld:C0013595 a ncit:C7057 .
  dgn-gda:DGN0246bc836df794205b69e2bf24bdda8a sio:SIO_000628 miriam-gene:2312 , lld:C0013595 ;
    a sio:SIO_001121 .
}
dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_provenance {
   dgn-np:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_assertion dcterms:description "[We performed a meta-analysis of 24 studies on FLG mutations and eczema involving 5,791 cases, 26,454 control subjects, and 1,951 families as well as 17 studies on asthma involving 3,138 cases, 17,164 control subjects, and 1,511 offspring.]. 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:19501237 ;
    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:NP226377.RAZUG9TRL2OpSlxj0XlOdoqoUNJvOaTQ-b3fe3RwQvgnw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:05+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" .
}