count	source_label	source_id	relationship	target_label	target_id	entity_type	solr_id	publication_id	sentences
4	AB34G_ARATH	UNIPROT:Q7PC87	activates		CHEBI:22990	Chemical	b325bdaa-45e6-11f0-afc2-0050569a791b	10.1016/j.pbi.2022.102184	AtABCG34 mediates camalexin secretion onAlternaria brassicicolainfection [35], whereas AtABCG36 and AtABCG40 secrete camalexin in response to infection withBotrytis cinerea[36∗].
2	AB34G_ARATH	UNIPROT:Q7PC87	activates		CHEBI:16974	Chemical	93877aca-454f-11f0-afc2-0050569a791b	10.1016/j.jbiotec.2022.05.002	Inoculation of PD-R6 strain reduced the stress ethylene level under salt stress and also increased the IAA production and root length in canola plants.
2	AB34G_ARATH	UNIPROT:Q7PC87	activates		CHEBI:22990	Chemical	a1f4407c-351a-11e8-87fd-001a4a160176	PMC5514727	This result is consistent with our explanation that the two proteins function in the same pathway of defense against the pathogen: That PAD3 catalyzes the biosynthesis of camalexin, whereas AtABCG34 mediates transport of camalexin.|||Second, expression of sGFP:ABCG34 in BY2 cells improved resistance to a toxic concentration of camalexin (Fig. 5B–D), suggesting that AtABCG34 mediates the removal of camalexin from the BY2 cells.
1	AB34G_ARATH	UNIPROT:Q7PC87	increases		CHEBI:22990	Chemical	a1f4407c-351a-11e8-87fd-001a4a160176	PMC5514727	These data suggest that AtABCG34 is necessary for camalexin secretion to the surface uponA.brassicicolainfection.
1	AB34G_ARATH	UNIPROT:Q7PC87	activates		GO:0006810	Phenotype	a1f4407c-351a-11e8-87fd-001a4a160176	PMC5514727	This result is consistent with our explanation that the two proteins function in the same pathway of defense against the pathogen: That PAD3 catalyzes the biosynthesis of camalexin, whereas AtABCG34 mediates transport of camalexin.
1	AB34G_ARATH	UNIPROT:Q7PC87	activates		MESH:D060467	Phenotype	a1f4407c-351a-11e8-87fd-001a4a160176	PMC5514727	These results suggest that AtABCG34 contributes to the disease resistance in naturally occurring genetic variants.
1		UNIPROT:P0DJY6	activates	AB34G_ARATH	UNIPROT:Q7PC87	Protein	a1f4407c-351a-11e8-87fd-001a4a160176	PMC5514727	When treated withA.brassicicola, the green fluorescence of sGFP:ABCG34 increased continuously until 24 h postinoculation (hpi) (Fig. 3GandH), indicating induction of AtABCG34 by the pathogen, in agreement with the results of our qRT-PCR analysis (Fig. 3CandFig.
1		UNIPROT:Q94A18	decreases	AB34G_ARATH	UNIPROT:Q7PC87	Protein	2d9272be-ae95-11ec-ae7b-0050569a1f61	PMCPMC8624133	Deletion of pdr1 caused significantly increased transcript level of pdr2 and pdr6, while the lack of pdr6 resulted significantly increased transcript level of pdr1.