@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs> .
@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:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_head {
  this: np:hasAssertion dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_assertion ;
    np:hasProvenance dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_provenance ;
    np:hasPublicationInfo dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_assertion a np:Assertion .
  dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_provenance a np:Provenance .
  dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
  dgn-gda:DGN15bb2f26259a1a1bc45aff22aa81cc2d sio:SIO_000628 miriam-gene:4524 , lld:C0005684 ;
    a sio:SIO_001121 .
}
dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_provenance {
  dgn-np:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_assertion dcterms:description "[We performed a case-control study of 158 bladder transitional cell carcinoma (TCC) cases and 316 controls to investigate the association between methylenetetrahydrofolate reductase (MTHFR) C677T, A1298G, and G1793A polymorphisms and bladder cancer susceptibility by polymerase chain reaction restriction fragment length polymorphism (PCR-RLFP) technique.]. 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:21046286 ;
    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:NP488377.RA-asLxufhhrus-MXKeGtFNcZwlJco-1O8jjJ6liCphIs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+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" .
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}