@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8> .
@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:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_head {
  this: np:hasAssertion dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion;
    np:hasProvenance dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance;
    np:hasPublicationInfo dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion a np:Assertion .
  
  dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance a np:Provenance .
  
  dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion {
  miriam-gene:215 a ncit:C16612 .
  
  lld:C0011303 a ncit:C7057 .
  
  dgn-gda:DGN3e72a03a8c30cea5c876d1e5fc3169c6 sio:SIO_000628 miriam-gene:215, lld:C0011303;
    a sio:SIO_001121 .
}

dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance {
  dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion dcterms:description
      "[X-linked adrenoleukodystrophy (ALD), an inherited demyelinating disorder of the central nervous system, can be corrected by allogeneic bone marrow transplantation, likely due to the turnover of brain macrophages that are bone marrow derived.]. 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:12668127;
    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:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:05+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" .
}