@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs> .
@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:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_head {
  this: np:hasAssertion dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_assertion ;
    np:hasProvenance dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_provenance ;
    np:hasPublicationInfo dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_assertion a np:Assertion .
  dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_provenance a np:Provenance .
  dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_assertion {
  miriam-gene:10217 a ncit:C16612 .
  lld:C1168401 a ncit:C7057 .
  dgn-gda:DGNa454afb0fd101c8ac9a9110e220d83f5 sio:SIO_000628 miriam-gene:10217 , lld:C1168401 ;
    a sio:SIO_001121 .
}
dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_provenance {
  dgn-np:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_assertion dcterms:description "[To understand the association between candidate tumor suppressor genes (TSGs) human mismatch repair protein homologue 1 (hMLH1), AP20 region gene 1 (APRG1), integrin alpha RLC (ITGA9), RB1 serine phosphates from human chromosome 3 (RBSP3) at chromosomal 3p22.3 region and development of head and neck squamous cell carcinoma (HNSCC), alterations (deletion/promoter methylation/expression) of these genes were analyzed in 65 dysplastic lesions and 84 HNSCC samples.]. 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:20412120 ;
    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:NP889190.RAmjAH5Kg1rv7hEmUlEVE8S2azXc6QNGskgGvY2HfhWxs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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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}