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- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion type Assertion NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_head.
- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion wasGeneratedBy ECO_0000203 NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_provenance.
- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion wasDerivedFrom befree-20140225 NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_provenance.
- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion SIO_000772 21725307 NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_provenance.
- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion evidence source_evidence_literature NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_provenance.
- NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_assertion description "[Consistent with a shared function for complex components, we identified a mutation in TCTN1 that causes Joubert syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598527.RAP8S_7M3GxeYRuMozUJ-NIZGJ9RIaA1A7gD1UQlE2-KI130_provenance.