@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8> .
@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:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_head {
  this: np:hasAssertion dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_assertion ;
    np:hasProvenance dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_provenance ;
    np:hasPublicationInfo dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_assertion a np:Assertion .
  dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_provenance a np:Provenance .
  dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  lld:C0005695 a ncit:C7057 .
  dgn-gda:DGNe0f8b1542b8e5eca6f496f650dbc3743 sio:SIO_000628 miriam-gene:26191 , lld:C0005695 ;
    a sio:SIO_001121 .
}
dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_provenance {
  dgn-np:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_assertion dcterms:description "[Furthermore, we have shown that 12p, a region of agreement between CGH and PEP harbors RhoGDI2, a candidate gene, the expression of which inversely correlates with bladder tumor progression, demonstrating the usefulness of this multimodal approach in identifying promising genetic changes that may be responsible for the invasive phenotype.]. 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:12460916 ;
    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:NP307835.RA_G9zcCbu_UHWzZZsRE4XLIobjJSWGjEFmbVE87Avon8130_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> ;
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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}