@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs> .
@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:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_head {
  this: np:hasAssertion dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion ;
    np:hasProvenance dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance ;
    np:hasPublicationInfo dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion a np:Assertion .
  dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance a np:Provenance .
  dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion {
  miriam-gene:6280 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN753574605e977be0ab14f43d3c54d110 sio:SIO_000628 miriam-gene:6280 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance {
  dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion dcterms:description "[In addition, whereas most of the carcinomas showed allelic loss for all three of the probes, indicating a large-scale deletion, several of the carcinomas exhibited losses for only one or two of the probes, thus making it possible, along with the cytogenetic data, to define the least common region of deletion to 3p13----p14.2.]. 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:1686726 ;
    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:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:50+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" .
}