@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys> .
@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:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_head {
  this: np:hasAssertion dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion ;
    np:hasProvenance dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance ;
    np:hasPublicationInfo dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion a np:Assertion .
  dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance a np:Provenance .
  dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion {
  miriam-gene:1950 a ncit:C16612 .
  lld:C0026986 a ncit:C7057 .
  dgn-gda:DGN4b2b73923d86fa19c251db023ae38ccb sio:SIO_000628 miriam-gene:1950 , lld:C0026986 ;
    a sio:SIO_001121 .
}
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance {
  dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion dcterms:description "[Using a probe specific for erb B oncogene, which encodes a truncated form of the EGF receptor, we examined RNA and DNA derived from bone marrow and peripheral blood mononuclear cells from three patients with myelodysplastic syndromes (MDS) and one with acute lymphocytic leukemia (ALL), all bearing an abnormal clone in their bone marrow with a similar unbalanced 1;7 translocation.]. 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:3464613 ;
    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:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}