@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:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_head { this: np:hasAssertion dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_assertion; np:hasProvenance dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_provenance; np:hasPublicationInfo dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_publicationInfo; a np:Nanopublication . dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_assertion a np:Assertion . dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_provenance a np:Provenance . dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_publicationInfo a np:PublicationInfo . } dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_assertion { miriam-gene:3342 a ncit:C16612 . lld:C0025149 a ncit:C7057 . dgn-gda:DGN724e1093186496043ec4977d4bab1bd0 sio:SIO_000628 miriam-gene:3342, lld:C0025149; a sio:SIO_001121 . } dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_provenance { dgn-np:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_assertion dcterms:description "[To map the breakpoints more precisely, we constructed a tiling-path matrix-CGH array covering chromosomal band 17p11.2 to the centromere and utilized it to delineate two small breakpoint intervals mapping at Mb 19.0 and 21.7 in seven of the medulloblastomas and in nine hematological neoplasias with i(17q).]. 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:16419060; 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:NP531516.RAgKMwifRjPpNoZcPagptCfTfVdRuOX8sIbokOEjGiroY130_publicationInfo { this: dcterms:created "2016-05-13T12:45:45+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" . }