@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:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_head { this: np:hasAssertion dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_assertion; np:hasProvenance dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_provenance; np:hasPublicationInfo dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_publicationInfo; a np:Nanopublication . dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_assertion a np:Assertion . dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_provenance a np:Provenance . dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_publicationInfo a np:PublicationInfo . } dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_assertion { miriam-gene:238 a ncit:C16612 . lld:C0027819 a ncit:C7057 . dgn-gda:DGNb5f19c84c6623763e6e875d49553efae sio:SIO_000628 miriam-gene:238, lld:C0027819; a sio:SIO_001122 . } dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_provenance { dgn-np:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_assertion dcterms:description "[We have selected seven ALK mutants identified in cell lines representative of a variety of human cancers based on position within the ALK protein, zygosity and frequency of detection including R1192Q, K1525E, C1021Y, R412C, A1252V, D1311A, K1518N and have compared their transformation capability in comparison to the published neuroblastoma-associated F1174L ALK mutant when expressed in immortalized p53(-/-) murine embryonic fibroblasts.]. 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:22086496; 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:NP939070.RAbO7ttkWnxMJvaKcbVGjf4WbWyI6g1bWFMoGLfdaTklU130_publicationInfo { this: dcterms:created "2016-05-13T12:48:50+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" . }