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- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion type Assertion NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_head.
- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion wasGeneratedBy ECO_0000218 NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_provenance.
- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion wasDerivedFrom uniprot-2016 NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_provenance.
- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion SIO_000772 10425035 NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_provenance.
- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion evidence source_evidence_curated NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_provenance.
- NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_assertion description "[Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294.RADXuOI7I9Q20EntOR-JVwmlg6L_4Q7-jY5ude2MtGd-s130_provenance.