@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs> .
@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:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_head {
  this: np:hasAssertion dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_assertion ;
    np:hasProvenance dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_provenance ;
    np:hasPublicationInfo dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_assertion a np:Assertion .
  dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_provenance a np:Provenance .
  dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  lld:C2981142 a ncit:C7057 .
  dgn-gda:DGN2512db165f1dfc451d4250b227390da2 sio:SIO_000628 miriam-gene:2187 , lld:C2981142 ;
    a sio:SIO_001121 .
}
dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_provenance {
  dgn-np:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_assertion dcterms:description "[Myelodysplastic syndromes (MDS) characterized by multilineage cytopenias and dysplasia but lacking an increase in blasts, with no Auer rods or monocytosis, do not exactly fit any of the categories of the French-American-British (FAB) classification of MDS and are often diagnosed as refractory anemia (RA), refractory anemia with ringed sideroblasts (RARS), or 'unclassifiable' MDS.]. 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:8558932 ;
    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:NP578588.RAlWvXBhUsqZ4EWycVwv4fK9h0jP5gJxU62xMpQJPTlDs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:48+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" .
}