@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA> .
@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:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_head {
  this: np:hasAssertion dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion;
    np:hasProvenance dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance;
    np:hasPublicationInfo dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion a np:Assertion .
  
  dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance a np:Provenance .
  
  dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion {
  miriam-gene:389421 a ncit:C16612 .
  
  lld:C0034012 a ncit:C7057 .
  
  dgn-gda:DGNe4730dcddb3d0b2a114caf4cb4ada612 sio:SIO_000628 miriam-gene:389421, lld:C0034012;
    a sio:SIO_001122 .
}

dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance {
  dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion dcterms:description
      "[Our results show that mutations in the coding region or 3 untranslated region miRNA recognition elements A and B of LIN28B do not underlie CDGP. Lack of any variation in the coding region of the gene suggests that LIN28B in developmental timing is so crucial that any changes in the conserved protein would probably be lethal.]. 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:20350940;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}