@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:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_head { this: np:hasAssertion dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_assertion; np:hasProvenance dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_provenance; np:hasPublicationInfo dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_publicationInfo; a np:Nanopublication . dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_assertion a np:Assertion . dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_provenance a np:Provenance . dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_assertion { miriam-gene:2322 a ncit:C16612 . lld:C0023467 a ncit:C7057 . dgn-gda:DGNe98dcde0ef3370d70392755eb965e106 sio:SIO_000628 miriam-gene:2322, lld:C0023467; a sio:SIO_001121 . } dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_provenance { dgn-np:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_assertion dcterms:description "[This novel D-HPLC-based procedure, which is optimized for identification of new point mutations in the catalytic and regulatory domains of FLT3 receptor, could potentially be useful for studies involving precise genotype determination, which could be critical for selection of innovative AML therapies targeting the FLT3 protein.]. 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:14500589; 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:NP413879.RAKvM3Y4AAGIB4GE7FstxQLSY2DtQ5fraXnNb3fqk2NhQ130_publicationInfo { this: dcterms:created "2016-05-13T12:44:52+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" . }