PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33879618-1	2021	DDX11 encodes an iron-sulfur cluster DNA helicase required for development, mutated, and overexpressed in cancers.	Iron	17-21	DEAD/H-box helicase 11	Homo sapiens	0-5	
24487782-4	2014	WABS is genetically linked to bi-allelic mutations in the ChlR1/DDX11 gene which encodes a protein of the conserved family of Iron-Sulfur (Fe-S) cluster DNA helicases.	Iron	139-143	DEAD/H-box helicase 11	Homo sapiens	58-63	
27107905-1	2016	FANCJ is a superfamily 2 DNA helicase, which also belongs to the iron-sulfur domain containing helicases that include XPD, ChlR1 (DDX11), and RTEL1.	Iron	65-69	DEAD/H-box helicase 11	Homo sapiens	123-128	
27107905-1	2016	FANCJ is a superfamily 2 DNA helicase, which also belongs to the iron-sulfur domain containing helicases that include XPD, ChlR1 (DDX11), and RTEL1.	Iron	65-69	DEAD/H-box helicase 11	Homo sapiens	130-135	
31287223-2	2019	The DDX11 gene codes for an iron-sulfur DNA helicase in the Superfamily 2 helicases and plays an important role in genomic stability and maintenance.	Iron	28-32	DEAD/H-box helicase 11	Homo sapiens	4-9	
28960803-3	2017	DDX11 encodes an iron-sulfur-containing DNA helicase, and mutations in this gene have been reported in the five WABS cases previously identified to date.	Iron	17-21	DEAD/H-box helicase 11	Homo sapiens	0-5	
24487782-4	2014	WABS is genetically linked to bi-allelic mutations in the ChlR1/DDX11 gene which encodes a protein of the conserved family of Iron-Sulfur (Fe-S) cluster DNA helicases.	Iron	139-143	DEAD/H-box helicase 11	Homo sapiens	64-69	
23935105-5	2013	FANCJ belongs to a conserved iron-sulfur (Fe S) cluster family of helicases important for genomic stability including XPD (nucleotide excision repair), DDX11 (sister chromatid cohesion), and RTEL (telomere metabolism), genetically linked to xeroderma pigmentosum/Cockayne syndrome, Warsaw breakage syndrome, and dyskeratosis congenita, respectively.	Iron	29-33	DEAD/H-box helicase 11	Homo sapiens	152-157	
23033317-1	2013	Mutations in the gene encoding the iron-sulfur-containing DNA helicase DDX11 (ChlR1) were recently identified as a cause of a new recessive cohesinopathy, Warsaw breakage syndrome (WABS), in a single patient with severe microcephaly, pre- and postnatal growth retardation, and abnormal skin pigmentation.	Iron	35-39	DEAD/H-box helicase 11	Homo sapiens	71-76	
23033317-1	2013	Mutations in the gene encoding the iron-sulfur-containing DNA helicase DDX11 (ChlR1) were recently identified as a cause of a new recessive cohesinopathy, Warsaw breakage syndrome (WABS), in a single patient with severe microcephaly, pre- and postnatal growth retardation, and abnormal skin pigmentation.	Iron	35-39	DEAD/H-box helicase 11	Homo sapiens	78-83