@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U> .
@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#> .
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  this: np:hasAssertion dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_assertion ;
    np:hasProvenance dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_provenance ;
    np:hasPublicationInfo dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_provenance a np:Provenance .
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}
dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_assertion {
  miriam-gene:3480 a ncit:C16612 .
  lld:C2939419 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_provenance {
  dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_assertion dcterms:description "[In this study, using the human colon cancer cell line HCT116, we find that established HCT116/IGF1-R transfectants exhibit a more aggressive transformed phenotype than the parental cell line, as demonstrated by their higher proliferation rate in response to IGF1, higher degree of anchorage-independent growth, resistance to serum deprivation-induced apoptosis, and higher migratory capability in a monolayer `wounding assay.` When injected into nude mice, HCT116/IGF1-R transfectants were highly invasive and produced distant metastases, whereas the parental cell did not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP833919.RAwuC305PXaIvahzY3rE5OUsEP954VJ-Bm6L_8C5BQr5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:30+02:00"^^xsd:dateTime ;
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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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