@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18> .
@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:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_head {
  this: np:hasAssertion dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion ;
    np:hasProvenance dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance ;
    np:hasPublicationInfo dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion a np:Assertion .
  dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance a np:Provenance .
  dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  lld:C0018923 a ncit:C7057 .
  dgn-gda:DGN4db9579c742c778a4ed24d06d403a435 sio:SIO_000628 miriam-gene:3845 , lld:C0018923 ;
    a sio:SIO_001121 .
}
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance {
  dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion dcterms:description "[We studied the occurrence of a specific ras mutation (Asp 13 c-Ki-ras) by oligonucleotide hybridization and the expression of the corresponding p21 protein in tumor tissue and serum by immunohistochemistry and immunoblotting with monoclonal antibodies in five individuals with heavy exposure to VC and resultant angiosarcomas of the liver (ASL).]. 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:8061177 ;
    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:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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" .
}