@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA> .
@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:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_head {
  this: np:hasAssertion dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion ;
    np:hasProvenance dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance ;
    np:hasPublicationInfo dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion a np:Assertion .
  dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance a np:Provenance .
  dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion {
  miriam-gene:140738 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN8c9443153b60697dd468c319309ed502 sio:SIO_000628 miriam-gene:140738 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance {
  dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion dcterms:description "[Conventional cytogenetic study of TSU-PR1 showed aneuploidy, ranging from 65 to 86 chromosome with a modal number of 80, and with 10 marker chromosomes, thus conventional cytogenetics cannot be used to determine which chromosomes or regions of chromosomes are critical in cancer development and progression of this cell line.]. 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:16271951 ;
    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:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:34+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" .
}