@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU> .
@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:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_head {
  this: np:hasAssertion dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_assertion;
    np:hasProvenance dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_provenance;
    np:hasPublicationInfo dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_assertion a np:Assertion .
  
  dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_provenance a np:Provenance .
  
  dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_assertion {
  miriam-gene:3214 a ncit:C16612 .
  
  lld:C0023522 a ncit:C7057 .
  
  dgn-gda:DGNb64b86fc6833273d3f606b42152cae8c sio:SIO_000628 miriam-gene:3214, lld:C0023522;
    a sio:SIO_001121 .
}

dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_provenance {
  dgn-np:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_assertion dcterms:description
      "[To evaluate the contribution of bone marrow (BM) cells to treat neurological disorders, we examined the effectiveness of BM cells expressing the homeobox B4 (HoxB4) gene to cure mice with metachromatic leukodystrophy (MLD) through transplantation.]. 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:20424597;
    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:NP615151.RA0HVHp7so3S8epMyqu8Jj9iRO08OJx_e4re5VRQH1_CU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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" .
}