@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ> .
@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:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_head {
  this: np:hasAssertion dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_assertion;
    np:hasProvenance dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_provenance;
    np:hasPublicationInfo dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_assertion a np:Assertion .
  
  dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_provenance a np:Provenance .
  
  dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_assertion {
  miriam-gene:730249 a ncit:C16612 .
  
  lld:C0242621 a ncit:C7057 .
  
  dgn-gda:DGN4b766fc16c5d2a3f79f9a55a190fde70 sio:SIO_000628 miriam-gene:730249, lld:C0242621;
    a sio:SIO_001121 .
}

dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_provenance {
  dgn-np:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_assertion dcterms:description
      "[These cells frequently become resistant to PALA through a mechanism that increases the aspartate transcarbamylase activity with no increase in CAD copy number, or they obtain one extra copy of CAD by forming an isochromosome 2p or by retaining an extra copy of chromosome 2.]. 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:9050862;
    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:NP768129.RAlVTW7gkPXaBqMSqsMAVKL8YaJqt8xtsXZAKvVcTqMuQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}