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- source_evidence_literature type ECO_0000212 NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_assertion description "[The evidences of our investigations show that MLH1 and MSH2 gene mutations have an equivalent etiopathological role both for Lynch syndrome and for MTS; hence, we propose a broadened clinical criteria for definition of Lynch syndrome that will include sebaceous adenoma, carcinoma, and keratoacanthoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_assertion evidence source_evidence_literature NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_assertion SIO_000772 16826164 NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_assertion wasDerivedFrom befree-2016 NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_assertion wasGeneratedBy ECO_0000203 NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.
- befree-2016 importedOn "2016-02-19" NP558722.RA_CUgEpKOwaEVZRCdejV1BElnJpbFrOY3AbRwtYRFMQU130_provenance.