@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM> .
@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:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_head {
  this: np:hasAssertion dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_assertion ;
    np:hasProvenance dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_provenance ;
    np:hasPublicationInfo dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_assertion a np:Assertion .
  dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_provenance a np:Provenance .
  dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_assertion {
  miriam-gene:6223 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
  dgn-gda:DGN95bead14ac62fe6d6d3e30941f8c5752 sio:SIO_000628 miriam-gene:6223 , lld:C0000768 ;
    a sio:SIO_001121 .
}
dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_provenance {
  dgn-np:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_assertion dcterms:description "[Using this database, important epidemiologic, clinical, and laboratory observations have been made with regard to the clinical presentation, the inheritance of DBA, the genetics of congenital malformations, the therapeutic outcome, including the efficacy of hematopoietic stem cell transplantation, and the recognition of DBA as a cancer predisposition syndrome.]. 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:11563775 ;
    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:NP194827.RA38-tp9TPM84KfKIcEK2wYXpcJhhLHr5fuzFGOZqgEGM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}