@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc> .
@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:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_head {
  this: np:hasAssertion dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_assertion ;
    np:hasProvenance dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_provenance ;
    np:hasPublicationInfo dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_assertion a np:Assertion .
  dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_provenance a np:Provenance .
  dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_assertion {
  miriam-gene:129831 a ncit:C16612 .
  lld:C0002895 a ncit:C7057 .
  dgn-gda:DGNb1237cc541d1e50d22ac9db3c69664f2 sio:SIO_000628 miriam-gene:129831 , lld:C0002895 ;
    a sio:SIO_001121 .
}
dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_provenance {
  dgn-np:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_assertion dcterms:description "[This study examined the theoretical availability of compatible unrelated umbilical cord blood (UCB) units for hematopoietic stem cell transplantation (HSCT) of children with sickle cell disease (SCD), matched for DRB1 at high resolution.]. 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:16394889 ;
    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:NP751565.RABZXCQ54z0McMjaD3UG4sKtW9V9Xc6_Y_h_qG_jczQWc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:35+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" .
}