@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc> .
@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:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_head {
  this: np:hasAssertion dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion;
    np:hasProvenance dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance;
    np:hasPublicationInfo dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion a np:Assertion .
  
  dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance a np:Provenance .
  
  dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion {
  miriam-gene:1471 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGNabb8455c9cbb56b92ee7a565224c88d8 sio:SIO_000628 miriam-gene:1471, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance {
  dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion dcterms:description
      "[Crossbreeding of CysBKO mice with either CysC-overexpressing transgenic mice or CysC-knockout mice demonstrates that clinical symptoms and neuropathologies, including motor coordination disorder, cerebellar atrophy, neuronal loss in the cerebellum and cerebral cortex, and gliosis caused by CysB deficiency, are rescued by CysC overexpression and exacerbated by CysC deficiency.]. 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:20889561;
    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:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}