@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:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_head { this: np:hasAssertion dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_assertion; np:hasProvenance dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_provenance; np:hasPublicationInfo dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_publicationInfo; a np:Nanopublication . dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_assertion a np:Assertion . dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_provenance a np:Provenance . dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_publicationInfo a np:PublicationInfo . } dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_assertion { miriam-gene:6776 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGN9d142fe51943f2ae02046a86d69c1a39 sio:SIO_000628 miriam-gene:6776, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_provenance { dgn-np:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_assertion dcterms:description "[We characterize fixation conditions suitable for accurate PP quantitation that are achievable in a clinical laboratory and illustrate the utility of in situ quantitation of PPs by quantum dot (QD) nanocrystals in two models: (1) a therapeutic model demonstrating effects of a targeted therapeutic (quantitative reduction of phospho-GSK3beta) in xenografts treated with enzastaurin; and (2) a diagnostic model that identifies elevated levels of nuclear phospho-STAT5 in routine bone marrow biopsies from patients with acute myeloid leukemia based on the presence of the activating FLT3-ITD mutation.]. 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:19332430; 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:NP729447.RA0pJfSC6jym6pffyyAptX_gIb5bLfPG0utlnE_M91KxY130_publicationInfo { this: dcterms:created "2016-05-13T12:47:16+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" . }