@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k> .
@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:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_head {
  this: np:hasAssertion dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion ;
    np:hasProvenance dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance ;
    np:hasPublicationInfo dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion a np:Assertion .
  dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance a np:Provenance .
  dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion {
  miriam-gene:11261 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGNe3785aef8a23e8dc1f0943b76b7bc832 sio:SIO_000628 miriam-gene:11261 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance {
  dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion dcterms:description "[To determine the contribution of these genes to the development of basal cell carcinomas we looked for evidence of allelic imbalance in 67 sporadic basal cell carcinoma specimens from Greek patients and screened 28 of them presenting loss of heterozygosity at 9p21-p22 for germline mutations in p16INK4a and p19ARF genes.]. 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:10998150 ;
    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:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}