@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI> .
@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:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_head {
  this: np:hasAssertion dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion ;
    np:hasProvenance dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance ;
    np:hasPublicationInfo dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion a np:Assertion .
  dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance a np:Provenance .
  dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0029445 a ncit:C7057 .
  dgn-gda:DGNdeb44c6856c8c0b98bc6c6e9099de2c4 sio:SIO_000628 miriam-gene:4524 , lld:C0029445 ;
    a sio:SIO_001122 .
}
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance {
  dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_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:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}