@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs> .
@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:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_head {
  this: np:hasAssertion dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion ;
    np:hasProvenance dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance ;
    np:hasPublicationInfo dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion a np:Assertion .
  dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance a np:Provenance .
  dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion {
  miriam-gene:4830 a ncit:C16612 .
  lld:C0014170 a ncit:C7057 .
  dgn-gda:DGNc821e3511338afaa5308596eec263077 sio:SIO_000628 miriam-gene:4830 , lld:C0014170 ;
    a sio:SIO_001122 .
}
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance {
  dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion dcterms:description "[Heterozygous genotypes TC in rs16949649 and CT in rs2302254 of nm23-H1 promoter are potential susceptibility factors for endometrial cancer in Taiwan women. Once having the endometrial cancer, Taiwan women with variant homozygote CC in rs1694964 were at less risk to have non-endometrioid type, while women with variant homozygote TT in rs2302254 tended to have advanced stage cancer.]. 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:20599259 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}