@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q> .
@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:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_head {
  this: np:hasAssertion dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_assertion ;
    np:hasProvenance dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_assertion a np:Assertion .
  dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_provenance a np:Provenance .
  dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0019562 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_provenance {
  dgn-np:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_assertion dcterms:description "[We have extended our LOH analysis of chromosome 3p to include 102 ovarian tumor specimens (29 and 73 samples were previously examined for LOH of chromosome 3p and 17 markers, respectively), using additional polymorphic markers, to assess the coordinate LOH of loci representing the three chromosome 3p minimal regions of deletions [von Hippel-Lindau syndrome (VHL), thyroid hormone receptor beta, and fragile histidine triad (FHIT)] and LOH of other important loci [tumor protein 53 (TP53), breast cancer 1 early onset (BRCA1), breast cancer 2 early onset, retinoblastoma 1, ornithine carbamoyltransferase, and androgen receptor] or somatic mutations in TP53.]. 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:12112314 ;
    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:NP652949.RAkr2AlP9xY5GmGNnt43q0Dngk76XRPQaOazSjA25St0Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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> ;
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}