@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_head {
   this: np:hasAssertion dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_assertion ;
    np:hasProvenance dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_provenance ;
    np:hasPublicationInfo dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_assertion a np:Assertion .
  dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_provenance a np:Provenance .
  dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_assertion {
   miriam-gene:7490 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGN0b5e6d13fb9cb32abfcc227ff5e98fad sio:SIO_000628 miriam-gene:7490 , lld:C0376358 ;
    a sio:SIO_001121 .
}
dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_provenance {
   dgn-np:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_assertion dcterms:description "[Spontaneous deletion of portions of human chromosome 11 in some of the clones delineated the minimal portion of human chromosome 11 capable of suppressing prostatic cancer metastases as the region between 11p11.2-13 but not including the Wilms' tumor-1 locus.]. 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:1596907 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP778413.RAnLmqhK20sWzop5juAi9ME0zR0hyfZQty4wJn4QD_XFg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:30+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}