@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_head {
  this: np:hasAssertion dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_assertion;
    np:hasProvenance dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_provenance;
    np:hasPublicationInfo dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_assertion a np:Assertion .
  
  dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_provenance a np:Provenance .
  
  dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_assertion {
  miriam-gene:7096 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
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dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_provenance {
  dgn-np:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_assertion dcterms:description
      "[We noted: (a) a significant difference in the frequency of A11 (20.5% versus 10.2%; P &lt; 0.05) allele between melanoma patients and the North American Caucasian population; (b) a significantly higher frequency of A11 phenotype among responders (40.5%) than in the melanoma patient population (20.5%; P &lt; 0.01), which was even more obvious among patients responding to TIL therapy (47.4% versus 22.1%; P &lt; 0.05); within TIL patients, responders also had an increased frequency of A19 (42.1% versus 25.6%; P &lt; 0.05); (c) a correlation between the number of TILs received and response rate (P &lt; 0.005); and (d) an association between DR4 haplotype and decreased tolerance to IL-2 among the patients receiving TILs (P = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP739821.RAlCLiWEjAFnWKYY79EibEUjC0gSH1_pnYpUkSG0dVsS0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:06+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetv3.0rdf;
    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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  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}