@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k> .
@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:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_head {
  this: np:hasAssertion dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion;
    np:hasProvenance dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance;
    np:hasPublicationInfo dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion a np:Assertion .
  
  dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance a np:Provenance .
  
  dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion {
  miriam-gene:55743 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN1c2b2f0c9c76e1d82273910e657ecb59 sio:SIO_000628 miriam-gene:55743, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance {
  dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion dcterms:description
      "[Notably, decreased CHFR expression resulted in the acquisition of many phenotypes associated with malignant progression, including accelerated growth rates, higher mitotic index, enhanced invasiveness, increased motility, greater aneuploidy, and amplified colony formation in soft agar, further supporting the role of CHFR as a tumor suppressor in breast cancer.]. 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:17596595;
    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:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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" .
}