PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
22639907-1	2012	Epidermolysis bullosa simplex (EBS) is mainly caused by mutations in the KRT5 and KRT14 genes.	simplex	22-29	keratin 5	Homo sapiens	73-77
23289980-1	2013	BACKGROUND: Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA).	simplex	114-121	plectin	Homo sapiens	37-44
23289980-1	2013	BACKGROUND: Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA).	simplex	114-121	plectin	Homo sapiens	51-55
22639907-1	2012	Epidermolysis bullosa simplex (EBS) is mainly caused by mutations in the KRT5 and KRT14 genes.	simplex	22-29	keratin 14	Homo sapiens	82-87
20199538-1	2010	BACKGROUND: Basal epidermolysis bullosa simplex (EBS) is a hereditary skin blistering disorder resulting in most cases from missense mutations in the keratin 5 (KRT5) or keratin 14 (KRT14) genes.	simplex	40-47	keratin 5	Homo sapiens	150-159
21490615-1	2011	Epidermolysis bullosa simplex (EBS) is a blistering skin disease caused by mutations in keratin genes (KRT5 or KRT14), with no existing therapies.	simplex	22-29	keratin 5	Homo sapiens	103-107
21490615-1	2011	Epidermolysis bullosa simplex (EBS) is a blistering skin disease caused by mutations in keratin genes (KRT5 or KRT14), with no existing therapies.	simplex	22-29	keratin 14	Homo sapiens	111-116
22747925-1	2012	We report a case of epidermolysis bullosa simplex (EBS) associated with a family cluster of EBS and a novel KRT5 mutation.	simplex	42-49	keratin 5	Homo sapiens	108-112
21593775-4	2011	Epidermolysis bullosa simplex (EBS) is a genodermatosis resulting from KRT5 or KRT14 mutations.	simplex	22-29	keratin 5	Homo sapiens	71-75
21593775-4	2011	Epidermolysis bullosa simplex (EBS) is a genodermatosis resulting from KRT5 or KRT14 mutations.	simplex	22-29	keratin 14	Homo sapiens	79-84
20199538-1	2010	BACKGROUND: Basal epidermolysis bullosa simplex (EBS) is a hereditary skin blistering disorder resulting in most cases from missense mutations in the keratin 5 (KRT5) or keratin 14 (KRT14) genes.	simplex	40-47	keratin 5	Homo sapiens	161-165
20199538-1	2010	BACKGROUND: Basal epidermolysis bullosa simplex (EBS) is a hereditary skin blistering disorder resulting in most cases from missense mutations in the keratin 5 (KRT5) or keratin 14 (KRT14) genes.	simplex	40-47	keratin 14	Homo sapiens	170-180
20199538-1	2010	BACKGROUND: Basal epidermolysis bullosa simplex (EBS) is a hereditary skin blistering disorder resulting in most cases from missense mutations in the keratin 5 (KRT5) or keratin 14 (KRT14) genes.	simplex	40-47	keratin 14	Homo sapiens	182-187
10782015-1	2000	A novel missense mutation was detected in the L12 region of keratin 5 (K5) in a Slovene family diagnosed with a Weber-Cockayne variant of epidermolysis bullosa simplex (EBS).	simplex	160-167	keratin 5	Homo sapiens	60-69
20128788-1	2010	BACKGROUND: Epidermolysis bullosa simplex (EBS) is a mechanobullous skin fragility disease characterized by cytolysis of basal keratinocytes and intraepidermal blistering often caused by mutations in keratin genes (KRT5 or KRT14).	simplex	34-41	keratin 5	Homo sapiens	215-219
20128788-1	2010	BACKGROUND: Epidermolysis bullosa simplex (EBS) is a mechanobullous skin fragility disease characterized by cytolysis of basal keratinocytes and intraepidermal blistering often caused by mutations in keratin genes (KRT5 or KRT14).	simplex	34-41	keratin 14	Homo sapiens	223-228
17581617-1	2007	Epidermolysis bullosa simplex (EBS) is a skin disorder caused by mutations in keratin (K) 5 or K14 genes.	simplex	22-29	keratin 14	Mus musculus	95-98
10782015-1	2000	A novel missense mutation was detected in the L12 region of keratin 5 (K5) in a Slovene family diagnosed with a Weber-Cockayne variant of epidermolysis bullosa simplex (EBS).	simplex	160-167	keratin 5	Homo sapiens	71-73
20060687-1	2010	BACKGROUNDS: Epidermolysis bullosa simplex (EBS) is a group of hereditary bullous disorders caused by mutations in the keratin genes KRT5 and KRT14.	simplex	35-42	keratin 5	Homo sapiens	133-137
20060687-1	2010	BACKGROUNDS: Epidermolysis bullosa simplex (EBS) is a group of hereditary bullous disorders caused by mutations in the keratin genes KRT5 and KRT14.	simplex	35-42	keratin 14	Homo sapiens	142-147
16882168-1	2006	BACKGROUND: Epidermolysis bullosa simplex (EBS) comprises a group of hereditary bullous diseases characterized by intraepidermal blistering caused by mutations in either keratin gene, KRT5 or KRT14.	simplex	34-41	keratin 5	Homo sapiens	184-188
16882168-1	2006	BACKGROUND: Epidermolysis bullosa simplex (EBS) comprises a group of hereditary bullous diseases characterized by intraepidermal blistering caused by mutations in either keratin gene, KRT5 or KRT14.	simplex	34-41	keratin 14	Homo sapiens	192-197
15215887-3	2004	Epidermolysis bullosa simplex (EBS) is a genetic skin fragility disorder caused by mutations in the genes for keratins K5 or K14, the intermediate filaments present in the basal cells of the epidermis.	simplex	22-29	keratin 14	Homo sapiens	125-128