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- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion type Assertion NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_head.
- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion wasGeneratedBy ECO_0000203 NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_provenance.
- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion wasDerivedFrom befree-2016 NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_provenance.
- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion SIO_000772 23116563 NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_provenance.
- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion evidence source_evidence_literature NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_provenance.
- NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_assertion description "[An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1025342.RADIqs2UnJhI7M0KxNJO-PL1McWaytahd9qOr-uzaxubQ130_provenance.