@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k> .
@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:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_head {
  this: np:hasAssertion dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion ;
    np:hasProvenance dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance ;
    np:hasPublicationInfo dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion a np:Assertion .
  dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance a np:Provenance .
  dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion {
  miriam-gene:7161 a ncit:C16612 .
  lld:C0027651 a ncit:C7057 .
  dgn-gda:DGN6107920f4a30d04ef531b7e130cb4899 sio:SIO_000628 miriam-gene:7161 , lld:C0027651 ;
    a sio:SIO_001121 .
}
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance {
  dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion dcterms:description "[Since it has been proposed that especially neoplasias lacking p53 alterations might show a loss of heterozygosity at 1p35-1p36, we studied the frequency of p53 and p73 deletions in bone marrow mononuclear cells of 68 patients with MM, two patients with monoclonal gammopathy of undetermined significance and four patients with plasma cell leukemia.]. 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:10602435 ;
    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:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}