@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s> .
@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:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_head {
  this: np:hasAssertion dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_assertion;
    np:hasProvenance dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_provenance;
    np:hasPublicationInfo dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_assertion a np:Assertion .
  
  dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_provenance a np:Provenance .
  
  dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGN3b0bee565d4ae7f7a9721abf02cb5508 sio:SIO_000628 miriam-gene:3342, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_provenance {
  dgn-np:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_assertion dcterms:description
      "[In IDH lesions loss of heterozygosity (LOH) at various loci could be identified, and comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH) studies delivered evidence for DNA amplification on chromosomal region 20q13 in the early stage of IDH.However, little is currently known about genetic alterations in those premalignant lesions, and the chronology of genetic alterations and histopathological changes during carcinogenesis is mainly undiscovered.]. 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:12446956;
    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:NP648990.RAXdalogTwq5QHk6hXThKrMOfMnpLYLU1hDmhFgUD_Z8s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}