@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho> .
@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:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_head {
  this: np:hasAssertion dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion ;
    np:hasProvenance dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance ;
    np:hasPublicationInfo dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion a np:Assertion .
  dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance a np:Provenance .
  dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion {
  miriam-gene:4254 a ncit:C16612 .
  lld:C0002874 a ncit:C7057 .
  dgn-gda:DGN073fd7edbc3f3edcb9e6cb39a6b4d1f4 sio:SIO_000628 miriam-gene:4254 , lld:C0002874 ;
    a sio:SIO_001121 .
}
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance {
  dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion dcterms:description "[In order to investigate the levels of stem cell factor (SCF) and its receptor c-kit protein and mRNA in pediatric aplastic anemia (AA) and their relevance to the pathogenesis, immunocytochemical and in situ hybridization were utilized to detect the expression of SCF and its receptor c-kit gene protein and mRNA, respectively in 59 children with AA and 51 normal controls.]. 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:15934301 ;
    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:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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> ;
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}