@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_head {
  this: np:hasAssertion dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_assertion ;
    np:hasProvenance dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_provenance ;
    np:hasPublicationInfo dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_assertion a np:Assertion .
  dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_provenance a np:Provenance .
  dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGN7d5a687611d17a3ffaf1bd34728785da sio:SIO_000628 miriam-gene:7421 , lld:C0007222 ;
    a sio:SIO_001122 .
}
dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_provenance {
  dgn-np:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_assertion dcterms:description "[The Cdx2-GATA haplotype 1 allele was related to increased mortality risk, which may be partly explained by osteoporotic fractures. As the biological mechanism is uncertain and this study size is limited, our results should be interpreted as hypothesis gen]. 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:21051524 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP147940.RA9789MWjt052vVAQIHkxBINpbtpMEduJWu-IAfnQd0Po130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:03+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}