@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo> .
@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:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_head {
  this: np:hasAssertion dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_assertion ;
    np:hasProvenance dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_provenance ;
    np:hasPublicationInfo dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_assertion a np:Assertion .
  dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_provenance a np:Provenance .
  dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_assertion {
  miriam-gene:1403 a ncit:C16612 .
  lld:C0023890 a ncit:C7057 .
  dgn-gda:DGNbdb179b5409c2d55be0888846182788d sio:SIO_000628 miriam-gene:1403 , lld:C0023890 ;
    a sio:SIO_001121 .
}
dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_provenance {
  dgn-np:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_assertion dcterms:description "[Recently, a cirrhosis risk score (CRS) based on seven single-nucleotide polymorphisms was proposed as genetic predictor of cirrhosis in hepatitis C. To assess the role of CRS in predicting fibrosis progression in patients with initially no or minimal to moderate fibrosis, we investigated 271 untreated patients with chronic hepatitis C having initial liver biopsy showing METAVIR stage F0 (n = 104), F1 (n = 101), or F2 (n = 59) who had been followed up without antiviral therapies for at least 60 months (mean 108.5 +/- 71.5 months) and had a liver biopsy at the end of this observation period.]. 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:19676127 ;
    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:NP904976.RAIblonQzoa2T-8dYHiez1CnTrf4C3YtimvrBJafk6kxo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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> ;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}