@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:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_head { this: np:hasAssertion dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_assertion; np:hasProvenance dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_provenance; np:hasPublicationInfo dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_publicationInfo; a np:Nanopublication . dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_assertion a np:Assertion . dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_provenance a np:Provenance . dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_publicationInfo a np:PublicationInfo . } dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_assertion { miriam-gene:1236 a ncit:C16612 . lld:C0033027 a ncit:C7057 . dgn-gda:DGN66509871a82fee9e21ef3aa07e2bcef8 sio:SIO_000628 miriam-gene:1236, lld:C0033027; a sio:SIO_001121 . } dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_provenance { dgn-np:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_assertion dcterms:description "[In summary, the results show that the defects in the erythroid development in a subpopulation of patients with myelodysplasia is localized at an early stage of the erythroid differentiation and is associated with the persistent expression of the CD34 antigen and, in some cases, with the expression of Evi-1.]. 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:8695798; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP317711.RA4LcDo8tl_hX_NZgUGasIa-86xvzAe7r9bmxJRKeWMqA130_publicationInfo { this: dcterms:created "2015-08-25T14:40:42+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }