@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w> .
@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:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_head {
  this: np:hasAssertion dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_assertion ;
    np:hasProvenance dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_provenance ;
    np:hasPublicationInfo dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_assertion a np:Assertion .
  dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_provenance a np:Provenance .
  dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_assertion {
  miriam-gene:3320 a ncit:C16612 .
  lld:C0038644 a ncit:C7057 .
  dgn-gda:DGNc5814a3a1ab6e40135dc1f4e69d29f2f sio:SIO_000628 miriam-gene:3320 , lld:C0038644 ;
    a sio:SIO_001121 .
}
dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_provenance {
  dgn-np:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_assertion dcterms: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:NP514677.RAj-JIoJFf76k3SyMV7x0H6AQvJ5-uY5EUB4OPmIVJg1w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:06+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" .
}