@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw> .
@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:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_head {
  this: np:hasAssertion dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion;
    np:hasProvenance dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_provenance;
    np:hasPublicationInfo dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion a np:Assertion .
  
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  dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion {
  miriam-gene:54209 a ncit:C16612 .
  
  lld:C1857316 a ncit:C7057 .
  
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dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_provenance {
  dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion dcterms:description
      "[In this paper, we have studied polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), an early onset dementia with bone fractures caused by mutations in TYROBP (DAP12) and TREM2 genes, which encode important signaling molecules in human dendritic cells (DCs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:01+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;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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