@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U> .
@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:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_head {
  this: np:hasAssertion dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_assertion ;
    np:hasProvenance dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_provenance ;
    np:hasPublicationInfo dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_assertion a np:Assertion .
  dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_provenance a np:Provenance .
  dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_assertion {
  miriam-gene:5590 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN31bb47c4ff8b411f6a09842abf31d90d sio:SIO_000628 miriam-gene:5590 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_provenance {
  dgn-np:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_assertion dcterms:description "[Leukemia cells with low levels of MSH2 contained partial or complete somatic deletions of one to four genes that regulate MSH2 degradation (FRAP1 (also known as MTOR), HERC1, PRKCZ and PIK3C2B); we also found these deletions in individuals with adult acute lymphoblastic leukemia (16%) and sporadic colorectal cancer (13.5%).]. 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:21946537 ;
    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:NP155142.RAbUTPPgCQXidTW2_ZRCZSoJQ5VWqSGnIyfTKF3a2Al9U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}