@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY> .
@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#> .
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   this: np:hasAssertion dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_assertion ;
    np:hasProvenance dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_provenance ;
    np:hasPublicationInfo dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_provenance a np:Provenance .
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dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_assertion {
   miriam-gene:2934 a ncit:C16612 .
  lld:C0546837 a ncit:C7057 .
  dgn-gda:DGN1fa97f59d7676b5312fbb1d565be395e sio:SIO_000628 miriam-gene:2934 , lld:C0546837 ;
    a sio:SIO_001121 .
}
dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_provenance {
   dgn-np:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_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 ;
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  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:NP639496.RAbY9pvjzNvJ2jvv5wVY6GLqSG-D9AqMqgZDjSY3PAauY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:25+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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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