@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU> .
@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:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_head {
  this: np:hasAssertion dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_assertion;
    np:hasProvenance dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_provenance;
    np:hasPublicationInfo dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_assertion a np:Assertion .
  
  dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_provenance a np:Provenance .
  
  dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_assertion {
  miriam-gene:9353 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGNa4b35b13de8d09d43cc69649d38c44cb sio:SIO_000628 miriam-gene:9353, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_provenance {
  dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_assertion dcterms:description
      "[Moreover, overexpression of SLIT2 in SMMC-7721 cells induced by recombinant adenovirus suppressed cell growth, migration, and invasion, These results suggest that epigenetic inactivation of SLIT2 in HCC may be important in the development and progression of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:19100240;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:13+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" .
}