@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI> .
@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:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_head {
  this: np:hasAssertion dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_assertion ;
    np:hasProvenance dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_provenance ;
    np:hasPublicationInfo dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_assertion a np:Assertion .
  dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_provenance a np:Provenance .
  dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_assertion {
  miriam-gene:10383 a ncit:C16612 .
  lld:C0026499 a ncit:C7057 .
  dgn-gda:DGN4a60021dc54d061064070a5a4593b022 sio:SIO_000628 miriam-gene:10383 , lld:C0026499 ;
    a sio:SIO_001121 .
}
dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_provenance {
  dgn-np:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_assertion dcterms:description "[Loss of heterozygosity (LOH) and fluorescent in situ hybridization (FISH) analysis for chromosome 15 exhibited loss of the remaining copy of the beta(2)m gene in both cases but also hemizygous deletions and monosomies in 6 additional cases.]. 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:12471623 ;
    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:NP568898.RAuR2_iznEYEmLNS6h_vpJ2qXA1DbmszPKPNe8k17NueI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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" .
}