@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls> .
@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:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_head {
  this: np:hasAssertion dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_assertion ;
    np:hasProvenance dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_provenance ;
    np:hasPublicationInfo dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_assertion a np:Assertion .
  dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_provenance a np:Provenance .
  dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_assertion {
  miriam-gene:5054 a ncit:C16612 .
  lld:C0029445 a ncit:C7057 .
  dgn-gda:DGNafb380fb94d605898a5d6909bf743516 sio:SIO_000628 miriam-gene:5054 , lld:C0029445 ;
    a sio:SIO_001122 .
}
dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_provenance {
  dgn-np:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_assertion dcterms:description "[ Genotypes of PAI-1 4G/5G and MTHFR C677T or plasma concentrations of PAI-1 Ag and tHcy had no effect on the incidence of ONFH in Japanese subjects, unlike the results of studies performed in white subjects. The effect of genetic background on the pathologic conditions that developed in patients with postrenal transplant ONFH may differ according to race.]. 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:14742985 ;
    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:NP51886.RA3MbzTyl__6Mk1NnCcEsFtnpCKh-1ypHuT5GJ3o1ECls130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}