@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs> .
@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:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_head {
   this: np:hasAssertion dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_assertion ;
    np:hasProvenance dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_provenance ;
    np:hasPublicationInfo dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_assertion a np:Assertion .
  dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_provenance a np:Provenance .
  dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_assertion {
   miriam-gene:3447 a ncit:C16612 .
  lld:C0002878 a ncit:C7057 .
  dgn-gda:DGNc1d4280f98dd0019b269c567651141d5 sio:SIO_000628 miriam-gene:3447 , lld:C0002878 ;
    a sio:SIO_001121 .
}
dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_provenance {
   dgn-np:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_assertion dcterms:description "[Recently, genome-wide association studies (GWAS) in patients with chronic hepatitis C virus (HCV) infection have identified two functional single nucleotide polymorphisms (SNPs) in the inosine triphosphatase (ITPA) gene, that are associated strongly and independently with hemolytic anemia in patients exposed to pegylated-interferon (Peg-IFN) plus ribavirin (RBV) combined therapy.]. 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:23201294 ;
    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:NP185093.RAS2xal3qBblxPi2s5sohMkZuAxaQ3omZWJz1a9wuosBs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:41+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" .
}