PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24446489-1	2014	Idiopathic pulmonary arterial hypertension (PAH [IPAH]) is an insidious and potentially fatal disease linked to a mutation or reduced expression of bone morphogenetic protein receptor 2 (BMPR2).	ipah	49-53	bone morphogenetic protein receptor type 2	Homo sapiens	148-185	
24446489-1	2014	Idiopathic pulmonary arterial hypertension (PAH [IPAH]) is an insidious and potentially fatal disease linked to a mutation or reduced expression of bone morphogenetic protein receptor 2 (BMPR2).	ipah	49-53	bone morphogenetic protein receptor type 2	Homo sapiens	187-192	
23733703-3	2011	In addition, approximately 20% of patients with IPAH carry mutations in BMPR2.	ipah	48-52	bone morphogenetic protein receptor type 2	Homo sapiens	72-77	
19555857-3	2009	In addition, approximately 20% of patients with IPAH carry mutations in BMPR2.	ipah	48-52	bone morphogenetic protein receptor type 2	Homo sapiens	72-77	
27816994-1	2016	Mutations in the bone morphogenetic protein receptor (BMPR2) gene have been observed in 70 % of patients with heritable pulmonary arterial hypertension (HPAH) and in 11-40 % with idiopathic PAH (IPAH).	ipah	195-199	bone morphogenetic protein receptor type 2	Homo sapiens	54-59	
22129439-3	2012	As IPAH is associated with mutations of the bone morphogenetic protein receptor 2 (BMPR2) gene, the aim of this study was to investigate whether this association might also be found in patients with IPH.	ipah	3-7	bone morphogenetic protein receptor type 2	Homo sapiens	44-81	
22129439-3	2012	As IPAH is associated with mutations of the bone morphogenetic protein receptor 2 (BMPR2) gene, the aim of this study was to investigate whether this association might also be found in patients with IPH.	ipah	3-7	bone morphogenetic protein receptor type 2	Homo sapiens	83-88	
20096498-2	2010	METHOD: With the aim of increasing the knowledge of these genetic factors in our area, the BMPR2 gene was studied in 17 patients with PAH, 8 with FPAH and 9 with sporadic IPAH.	ipah	171-175	bone morphogenetic protein receptor type 2	Homo sapiens	91-96