@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY> .
@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 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:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_head {
  this: np:hasAssertion dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_assertion ;
    np:hasProvenance dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_provenance ;
    np:hasPublicationInfo dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_assertion a np:Assertion .
  dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_provenance a np:Provenance .
  dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_assertion {
  miriam-gene:80216 a ncit:C16612 .
  lld:C0023530 a ncit:C7057 .
  dgn-gda:DGN69fa09de75bccc8b974b22907b18c691 sio:SIO_000628 miriam-gene:80216 , lld:C0023530 ;
    a sio:SIO_001122 .
}
dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_provenance {
  dgn-np:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_assertion dc:description "[Our findings show that genetic variants in the microcephalin 1 locus are suggestively associated with the risk of epirubicin-induced ADRs and might be applicable in development of diagnostic system for predicting the risk of the ADRs, leading to better prognosis and quality of life for patients with cancer. However, these results should be considered preliminary until replicated in adequately larger powered and controlled samples.]. 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:21799462 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP96320.RAUJs5J30De9dZ0P_zXi70ZQPeQR1F3CoN83o4gQsvNsY130_publicationInfo {
  this: dc:created "2014-10-02T12:32:48+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc: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" .
}