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- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion type Assertion NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_head.
- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion description "[Escobar syndrome has been recently described as a prenatal form of myasthenia associated with recessive mutations in genes of the neuromuscular junction (CHRNG, CHRNA1, CHRND, RAPSN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_provenance.
- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion evidence source_evidence_literature NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_provenance.
- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion SIO_000772 19155175 NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_provenance.
- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion wasDerivedFrom befree-2016 NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_provenance.
- NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_assertion wasGeneratedBy ECO_0000203 NP715450.RA-kkiRHlE9hG7uHNGshEY1dukhi-SaIVR99HOfIPflWs130_provenance.