@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ> .
@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:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_head {
   this: np:hasAssertion dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_assertion ;
    np:hasProvenance dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_assertion a np:Assertion .
  dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_provenance a np:Provenance .
  dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_assertion {
   miriam-gene:2934 a ncit:C16612 .
  lld:C0152018 a ncit:C7057 .
  dgn-gda:DGNd666f1022acbe68721f83941d6e019ee sio:SIO_000628 miriam-gene:2934 , lld:C0152018 ;
    a sio:SIO_001121 .
}
dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_provenance {
   dgn-np:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_assertion dcterms:description "[To better define the deleted chromosomal loci and understand the genetic instability in EC tissues, we selected 12 microsatellite markers (D3S1232, D3S1238, D3S1289, D3S1480, D3S647, D3S966, D3S1317, D3S659, D9S156, D9S171, D9S176 and GSN) to examine 36 paired EC tissues for loss of heterozygosity (LOH) and microsatellite instability (MIN) on chromosomes 3 and 9.]. 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:8637728 ;
    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:NP757724.RA4QVIZydmDcMFPXjVIWQJz8x6614DOCEsP6EQ_QLIwIQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:39+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" .
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}