@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg> .
@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#> .
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  this: np:hasAssertion dgn-np:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_assertion ;
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    np:hasPublicationInfo dgn-np:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_assertion {
  miriam-gene:3059 a ncit:C16612 .
  lld:C0038013 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_provenance {
  dgn-np:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_assertion dcterms:description "[Polymorphisms associated in the allele frequencies test with severe BASFI/t in all classifications were: rs2542151 (p60 [P = .04], p65 [P = .04], p70 [P = .001] and p75 [P = .001]) and rs2254441 (p60 [P = .004], p65 [P = .02], p70 [P = .01] and p75 [P<.001]).. Genotype association, after adjustment for covariates, found an association in three of the four patients' classifications for rs2542151 and in two of the classifications for rs2254441.Forward logistic regression did not identify any model with a good predictive power for severe functional development.In our study we identified clinical factors and 24 polymorphisms associated with development of severe functional status in AS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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  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:NP559863.RAx_-stQn02Dm9Hq0wnYiGNiSbT5SsKZ4UZEwhvc8RHOg130_publicationInfo {
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    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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