@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8> .
@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:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_head {
  this: np:hasAssertion dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_assertion ;
    np:hasProvenance dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_provenance ;
    np:hasPublicationInfo dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_assertion a np:Assertion .
  dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_provenance a np:Provenance .
  dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_assertion {
  miriam-gene:27034 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGN2147a0b00e08925b4e703266769615b6 sio:SIO_000628 miriam-gene:27034 , lld:C0004096 ;
    a sio:SIO_001121 .
}
dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_provenance {
  dgn-np:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_assertion dcterms:description "[Using the sample of 107 families with at least two asthmatic siblings, as part of the EGEA study, we have investigated linkage to asthma (or atopy) and genetic heterogeneity according to the presence/absence of atopy (or asthma) using two approaches: (1) the triangle test statistic (TTS), which considers the identical by descent (IBD) distribution among affected sib-pairs discordant for another associated phenotype (eg asthmatic sib-pairs discordant for atopy) and (2) the predivided sample test (PST), which compares the IBD distribution of marker alleles between affected sib-pairs concordant and discordant for the associated phenotype.]. 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:12891379 ;
    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:NP900413.RAoKg55P8Bxp_biRnqzRIhQ00dKgcGXu040X8_FU_waX8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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> ;
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}