@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A> .
@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:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_head {
  this: np:hasAssertion dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion;
    np:hasProvenance dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance;
    np:hasPublicationInfo dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion a np:Assertion .
  
  dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance a np:Provenance .
  
  dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGN82e701e0e31dcdf0463b02895d6f6469 sio:SIO_000628 miriam-gene:4397, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance {
  dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion dcterms:description
      "[The distribution of ALlambda deposits in these 3 cases indicates that widespread subcortical vascular amyloidosis with leukoencephalopathy is a novel clinicopathologic entity distinguished from other cerebral diseases with local amyloid light chain deposition, including amyloidoma, leptomeningeal vascular amyloidosis, solitary intracerebral plasmacytoma, primary intracerebral lymphoma with plasmacytic differentiation, and multiple sclerosis with demyelination-associated amyloid deposition.]. 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:19225408;
    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:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:06+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" .
}