@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM> .
@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:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_head {
  this: np:hasAssertion dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_assertion;
    np:hasProvenance dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_provenance;
    np:hasPublicationInfo dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_assertion a np:Assertion .
  
  dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_provenance a np:Provenance .
  
  dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_assertion {
  miriam-gene:3417 a ncit:C16612 .
  
  lld:C1859088 a ncit:C7057 .
  
  dgn-gda:DGNe63c19a071d5cc865eed684bd0a5daa7 sio:SIO_000628 miriam-gene:3417, lld:C1859088;
    a sio:SIO_001121 .
}

dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_provenance {
  dgn-np:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_assertion dcterms:description
      "[Heterozygous mutations in the IDH1 occur in the majority of grade II and grade III gliomas and secondary glioblastomas and change the structure of the enzyme, which diminishes its ability to convert isocitrate (ICT) to alpha-ketoglutarate (alpha-KG) and provides it with a newly acquired ability to convert alpha-KG to R(-)-2-hydroxyglutarate [R(-)-2HG].]. 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:20510884;
    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:NP331444.RAJI4rt0ITmG3UM5RUeNeMpiJL7dvw5lH8mx8H4yyByNM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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" .
}