@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_head {
  this: np:hasAssertion dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_assertion;
    np:hasProvenance dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_provenance;
    np:hasPublicationInfo dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_assertion a np:Assertion .
  
  dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_provenance a np:Provenance .
  
  dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_assertion {
  miriam-gene:8892 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN1c9a843431d4845e0f3f7bc617c9120d sio:SIO_000628 miriam-gene:8892, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_provenance {
  dgn-np:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_assertion dcterms:description
      "[The large clinical spectrum observed from the more severe antenatal forms responsible for fetal death to milder adult forms with an onset after 16 years old and restricted to slow cognitive impairment have lead to the concept of eIF2B-related disorders.]. 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:20016818;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP782051.RAW3_JYAV74pq2_s8ikniMc1DM8YrcDZadNDtwo7Q6quw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:39+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}