@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo> .
@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:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_head {
   this: np:hasAssertion dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_assertion ;
    np:hasProvenance dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_provenance ;
    np:hasPublicationInfo dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_assertion a np:Assertion .
  dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_provenance a np:Provenance .
  dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_assertion {
   miriam-gene:925 a ncit:C16612 .
  lld:C0008679 a ncit:C7057 .
  dgn-gda:DGN15c95587ed4e372269da09f32785c7eb sio:SIO_000628 miriam-gene:925 , lld:C0008679 ;
    a sio:SIO_001121 .
}
dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_provenance {
   dgn-np:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_assertion dcterms:description "[A closer examination of CD8 escape mutations in additional persons with chronic disease indicated that not only did immune pressures frequently result in selection of identical amino acid substitutions in mutating epitopes, but mutating residues also correlated with highly polymorphic sites in both clade B and C viruses.]. 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:16227247 ;
    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:NP902885.RAhuNL1XE5N7f7TSWYpXFOTBGXMo_L2lj8lMQ0OTCASWo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:14+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" .
}