@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk> .
@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:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_head {
  this: np:hasAssertion dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_assertion ;
    np:hasProvenance dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_provenance ;
    np:hasPublicationInfo dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_assertion a np:Assertion .
  dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_provenance a np:Provenance .
  dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_assertion {
  miriam-gene:116833 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN38def0eb3defa31bb37818c2aa434474 sio:SIO_000628 miriam-gene:116833 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_provenance {
  dgn-np:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_assertion dcterms:description "[We found that these women were at significantly higher breast cancer risk if they carried alleles with at least 28 or 29 polyglutamine repeats at AIB1, compared with women who carried alleles with fewer polyglutamine repeats [odds ratio (OR), 1.59; 95% confidence interval (CI), 1.03-2.47 and OR, 2.85; 95% CI, 1.64-4.96, respectively].]. 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:11454686 ;
    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:NP382926.RA-FhH-R51jhnhfynB5gFIjwYlV9uYnBsRrHUPNGG36rk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:46+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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}