@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk> .
@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:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_head {
  this: np:hasAssertion dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_assertion ;
    np:hasProvenance dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_provenance ;
    np:hasPublicationInfo dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_assertion a np:Assertion .
  dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_provenance a np:Provenance .
  dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_assertion {
  miriam-gene:5914 a ncit:C16612 .
  lld:C0810364 a ncit:C7057 .
  dgn-gda:DGNefc6f8d192d84926a7347817104c6621 sio:SIO_000628 miriam-gene:5914 , lld:C0810364 ;
    a sio:SIO_001121 .
}
dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_provenance {
  dgn-np:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_assertion dcterms:description "[An association between a PstI restriction fragment length polymorphism or D17S579 microsatellite marker polymorphism of the RARA gene and NSCLP was previously suggested, but no nucleotide change that may influence the gene expression or the protein sequence has been reported to date.]. 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:12111375 ;
    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:NP452016.RAROwwnxzb-bAs1-C1Pk52kCQWgI9J2p_Rg51Rdy_25Bk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}