@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc> .
@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:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_head {
  this: np:hasAssertion dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion ;
    np:hasProvenance dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance ;
    np:hasPublicationInfo dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion a np:Assertion .
  dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance a np:Provenance .
  dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion {
  miriam-gene:9212 a ncit:C16612 .
  lld:C1623038 a ncit:C7057 .
  dgn-gda:DGN5ca686642489fbb432ec50a29c14631a sio:SIO_000628 miriam-gene:9212 , lld:C1623038 ;
    a sio:SIO_001121 .
}
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance {
  dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion dcterms:description "[The expression of Aurora B and splicing variant forms were screened in 125 HCC patients (94 chronic hepatitis with cirrhosis background liver specimens), 18 metastatic liver cancer patients and 16 normal liver specimens by cDNA microarray, reverse transcription -- polymerase chain reaction (RT-PCR) and Real time quantitative Reverse Transcription PCR (qRT-PCR).]. 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:19134008 ;
    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:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:32+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" .
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}