@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A> .
@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:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_head {
  this: np:hasAssertion dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_assertion ;
    np:hasProvenance dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_provenance ;
    np:hasPublicationInfo dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_assertion a np:Assertion .
  dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_provenance a np:Provenance .
  dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_assertion {
  miriam-gene:4827 a ncit:C16612 .
  lld:C0019196 a ncit:C7057 .
  dgn-gda:DGN11a135a0d2776b8a83c83b7a92e4b276 sio:SIO_000628 miriam-gene:4827 , lld:C0019196 ;
    a sio:SIO_001121 .
}
dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_provenance {
  dgn-np:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_assertion dcterms:description "[Previous surveys of the prevalences of genotypes of hepatitis C virus (HCV) in different populations have often used genotyping assays based upon analysis of amplified sequences from the 5' noncoding region (5'NCR), such as restriction fragment length polymorphism (RFLP) or hybridization with type-specific probes (e.g., InnoLipa).]. 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:8789027 ;
    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:NP413941.RAjpBRSi2FDPV3moPFRUcQtwTbFk6r8o3waOrBPVKTg1A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:06+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" .
}