@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY> .
@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 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:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_head {
  this: np:hasAssertion dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_assertion ;
    np:hasProvenance dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_provenance ;
    np:hasPublicationInfo dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_assertion a np:Assertion .
  dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_provenance a np:Provenance .
  dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_assertion {
  miriam-gene:3308 a ncit:C16612 .
  lld:C0038644 a ncit:C7057 .
  dgn-gda:DGN13fe8bc11d842e96f71099c87d451bd7 sio:SIO_000628 miriam-gene:3308 , lld:C0038644 ;
    a sio:SIO_001121 .
}
dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_provenance {
  dgn-np:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_assertion dc:description "[Comparison of the frequency of occurrence of restriction fragment length polymorphisms in control human DNAs and DNAs from infants dying from sudden infant death syndrome has indicated no significant difference in the case of restriction fragment length polymorphisms associated with the heat shock protein genes hsp70 and hsp90.]. 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:8957963 ;
    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:NP365906.RADvGXDMwFPsTHWwNL7tTlwsr_qtDv65Wvf--BiDI3_jY130_publicationInfo {
  this: dc:created "2014-10-02T12:35:34+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc: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" .
}