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PubMed:10229672 JSONTXT

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PMID_GLOBAL

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	554-558	DiseaseOrPhenotypicFeature	denotes	rich	0015404
T2	1003-1017	DiseaseOrPhenotypicFeature	denotes	ectopia lentis	0020236
T3	1525-1529	DiseaseOrPhenotypicFeature	denotes	rich	0015404
T4	1676-1680	DiseaseOrPhenotypicFeature	denotes	rich	0015404

DisGeNET5_variant_disease

Id	Subject	Object	Predicate	Lexical cue
10229672-6#73#79#geners137854464	1051-1057	geners137854464	denotes	E2447K
10229672-6#25#39#diseaseC0013581	1003-1017	diseaseC0013581	denotes	ectopia lentis
73#79#geners13785446425#39#diseaseC0013581	10229672-6#73#79#geners137854464	10229672-6#25#39#diseaseC0013581	associated_with	E2447K,ectopia lentis

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
10229672-6#138#161#gene1950	1116-1139	gene1950	denotes	epidermal growth factor
10229672-6#25#39#diseaseC0013581	1003-1017	diseaseC0013581	denotes	ectopia lentis
138#161#gene195025#39#diseaseC0013581	10229672-6#138#161#gene1950	10229672-6#25#39#diseaseC0013581	associated_with	epidermal growth factor,ectopia lentis

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	1116-1139	gene:1950	denotes	epidermal growth factor
T1	1003-1017	disease:C0013581	denotes	ectopia lentis
T2	1234-1245	gene:2200	denotes	fibrillin-1
T3	1003-1017	disease:C0013581	denotes	ectopia lentis
R1	T0	T1	associated_with	epidermal growth factor,ectopia lentis
R2	T2	T3	associated_with	fibrillin-1,ectopia lentis