@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA> .
@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:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_head {
  this: np:hasAssertion dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion ;
    np:hasProvenance dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance ;
    np:hasPublicationInfo dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion a np:Assertion .
  dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance a np:Provenance .
  dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion {
  miriam-gene:30009 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGN991e4648f2a2a8aaa2f49ee291465b2d sio:SIO_000628 miriam-gene:30009 , lld:C0004096 ;
    a sio:SIO_001122 .
}
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance {
  dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion dcterms:description "[In order to examine whether polymorphisms in the candidate gene, TBX21, located on chromosome 17q21.32, are related to the risk of human asthma phenotypes, we have searched for genetic variations in the human TBX21 gene and identified 24 single nucleotide polymorphisms (SNPs), including five novel SNPs, by direct sequencing in Japanese subjects.]. 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:15806396 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}