@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c> .
@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:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_head {
  this: np:hasAssertion dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_assertion ;
    np:hasProvenance dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_provenance ;
    np:hasPublicationInfo dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_assertion a np:Assertion .
  dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_provenance a np:Provenance .
  dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_assertion {
  miriam-gene:5340 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGNfe135df1d3c2083e5dbb7ecac58c9d76 sio:SIO_000628 miriam-gene:5340 , lld:C0004096 ;
    a sio:SIO_001121 .
}
dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_provenance {
  dgn-np:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_assertion dcterms:description "[A 3-phase procedure was used: (1) linkage and association analyses using 15 microsatellite markers spanning 14.4 mega base pairs (Mbps) on 19q13, (2) fine mapping of the refined region using 26 haplotype tagging single nucleotide polymorphisms (SNPs), and (3) dense gene analyses using 18 SNPs evaluated for association with asthma, bronchial hyperresponsiveness (BHR), FEV1, plasma urokinase plasminogen activator receptor (PLAUR), and rate of annual FEV1 decline in subjects with asthma.]. 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:19443020 ;
    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:NP499933.RAcxUT1XsWTG5_idl_2WmYdDJClHRxcL_OJ7B7MqmsO3c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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" .
}