@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE> .
@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:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_head {
  this: np:hasAssertion dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion;
    np:hasProvenance dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance;
    np:hasPublicationInfo dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion a np:Assertion .
  
  dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance a np:Provenance .
  
  dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0018939 a ncit:C7057 .
  
  dgn-gda:DGN4adcfaf08d723e93e6af50a3091b0740 sio:SIO_000628 miriam-gene:7157, lld:C0018939;
    a sio:SIO_001121 .
}

dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance {
  dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion dcterms:description
      "[In this review we will discuss: 5q- syndrome mouse models, the possible mechanisms underlying this blood disorder with respect to the candidate genes and comparisons with other ribosomopathies and the involvement of the p53 pathway in these diseases.]. 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:20980806;
    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:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:14+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" .
}