@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_head { this: np:hasAssertion dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_assertion; np:hasProvenance dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_provenance; np:hasPublicationInfo dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_publicationInfo; a np:Nanopublication . dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_assertion a np:Assertion . dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_provenance a np:Provenance . dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_publicationInfo a np:PublicationInfo . } dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_assertion { miriam-gene:947 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGN86ed04319d140b8d164992a2e137574c sio:SIO_000628 miriam-gene:947, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_provenance { dgn-np:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_assertion dcterms:description "[CD34+ bone marrow cells exhibit unique susceptibility to the development of specific chromosome aberrations that have been identified as the earliest structural changes occurring in the development of secondary myelodysplastic syndrome and acute myelogenous leukemia.]. 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:10706073; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP277320.RAA-5cDD6P6eDAjxu334Pcs0kaRncWsnL9v7mXM7AEvHs130_publicationInfo { this: dcterms:created "2016-05-13T12:43:51+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }