@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ> .
@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:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_head {
  this: np:hasAssertion dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_assertion ;
    np:hasProvenance dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_provenance a np:Provenance .
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}
dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_assertion {
  miriam-gene:3303 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGN3f1bbafad25901bf142d19d5e1eeabb4 sio:SIO_000628 miriam-gene:3303 , lld:C0023418 ;
    a sio:SIO_001122 .
}
dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_provenance {
  dgn-np:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_assertion dcterms:description "[To systematically evaluate their associations with childhood acute lymphoblastic leukemia (ALL), we examined the three functional single nucleotide polymorphisms (SNPs) rs2227956 (T493M) in HSPA1L, rs1043618 in HSPA1A 5'UTR, and rs1061581 (Q351Q) in HSPA1B by TaqMan assays or polymerase chain reaction-restriction fragment length polymorphism in 114 ALL cases and 414 controls from Wales (UK), in 100 Mexican Mestizo ALL cases and 253 controls belonging to the same ethnic group, and in a panel of 82 HLA-typed reference cell line samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
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  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:NP73257.RA9dwPbRJNNyJeMvjBe8uB_8P0Xbe1xdtTBxQ4JCEdMXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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    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> ;
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