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PubMed:9168438 JSONTXT

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PennBioIE

Id	Subject	Object	Predicate	Lexical cue
T1	0-5	protein	denotes	c-kit
T2	6-20	protein	denotes	Point mutation
T3	267-295	protein	denotes	hematopoietic growth factors
T4	307-321	protein	denotes	erythropoietin
T5	323-337	protein	denotes	thrombopoietin
T6	342-358	protein	denotes	stem cell factor
T7	360-363	protein	denotes	SCF
T8	366-369	protein	denotes	SCF
T9	386-400	protein	denotes	c-kit receptor
T10	406-421	protein	denotes	tyrosine kinase
T11	462-467	protein	denotes	c-kit
T12	559-573	protein	denotes	point mutation
T13	612-620	protein	denotes	codon 52
T14	622-625	protein	denotes	Asp
T15	628-631	protein	denotes	Asn
T16	777-780	protein	denotes	SCF
T17	781-786	protein	denotes	c-kit

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	307-321	gene:2056	denotes	erythropoietin
T1	229-232	disease:C0027022	denotes	MPD
R1	T0	T1	associated_with	erythropoietin,MPD

DisGeNET5_variant_disease

Id	Subject	Object	Predicate	Lexical cue
9168438-5#63#76#geners121913505	618-631	geners121913505	denotes	52 (Asp-->Asn
9168438-5#110#131#diseaseC0001815	665-686	diseaseC0001815	denotes	primary myelofibrosis
9168438-5#145#173#diseaseC0023473	700-728	diseaseC0023473	denotes	chronic myelogenous leukemia
63#76#geners121913505110#131#diseaseC0001815	9168438-5#63#76#geners121913505	9168438-5#110#131#diseaseC0001815	associated_with	52 (Asp-->Asn,primary myelofibrosis
63#76#geners121913505145#173#diseaseC0023473	9168438-5#63#76#geners121913505	9168438-5#145#173#diseaseC0023473	associated_with	52 (Asp-->Asn,chronic myelogenous leukemia