@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE> .
@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:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_head {
  this: np:hasAssertion dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion ;
    np:hasProvenance dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_provenance ;
    np:hasPublicationInfo dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion a np:Assertion .
  dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_provenance a np:Provenance .
  dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  lld:C0280100 a ncit:C7057 .
  dgn-gda:DGN30c97280d721a4e3eefa973de93d1937 sio:SIO_000628 miriam-gene:2272 , lld:C0280100 ;
    a sio:SIO_001121 .
}
dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_provenance {
  dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion dcterms:description "[To evaluate the loss of C3CER1 in various human tumor types, we conducted loss of heterozygosity (LOH) analysis of 576 human solid tumors from 10 different tissues and compared the frequency of deletion in the C3CER1 area to that in two other regions on 3p: the FHIT/FRA3B region, at 3p14.2, and the VHL region, at 3p25.3.]. 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:15334546 ;
    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:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}