@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM> .
@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:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_head {
  this: np:hasAssertion dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion ;
    np:hasProvenance dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance ;
    np:hasPublicationInfo dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion a np:Assertion .
  dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance a np:Provenance .
  dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion {
  miriam-gene:338386 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN8ad0c5573c50428db59048c196e23ee4 sio:SIO_000628 miriam-gene:338386 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance {
  dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion dcterms:description "[These findings suggest that: (a) the amplification produces c-erbB-2 in the HSR form generally early in the carcinogenesis of gastric adenocarcinomas; and (b) in the process of cancer development, the amplified gene is lost in some cancer cells by uneven segregation of HSR in mitosis, whereas in others, it is kept in HSR or translocated to other chromosomal positions, thereby preserving overexpression of c-erbB-2 protein.]. 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:9520947 ;
    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:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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" .
}