@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU> .
@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:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_head {
  this: np:hasAssertion dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion ;
    np:hasProvenance dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance ;
    np:hasPublicationInfo dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion a np:Assertion .
  dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance a np:Provenance .
  dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion {
  miriam-gene:30816 a ncit:C16612 .
  lld:C1458156 a ncit:C7057 .
  dgn-gda:DGN189fd9fe75c5d84c7784b6a20fb15957 sio:SIO_000628 miriam-gene:30816 , lld:C1458156 ;
    a sio:SIO_001121 .
}
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance {
  dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion dcterms:description "[This finding suggests that nucleotide mutations in the envelope region of the viral genome may be responsible for the recurrent hepatic injury attributed to recurrence of viremia in patients with hepatitis C. From these aspects, the serial divergence of the virus genome in infected individuals, especially in the region encoding the viral envelope protein, may possibly play an important role in developing chronic infection of hepatitis C virus.]. 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:1330930 ;
    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:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:13+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" .
}