Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_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." NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_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." NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP768590.RAXS3AOTKrWTFGvEiWA5D9Ndeyycq59-8Zb9U4ETlfJ8c130_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." NP768590.RAXS3AOTKrWTFGvEiWA5D9Ndeyycq59-8Zb9U4ETlfJ8c130_provenance.
- 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." provenance.
- 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." provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_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." NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314611.RAgDNsV1bhM-mW7pzbM3h7zJ1CX8UJ0v7jFDBSa3-_6Gg130_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." NP314611.RAgDNsV1bhM-mW7pzbM3h7zJ1CX8UJ0v7jFDBSa3-_6Gg130_provenance.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_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." NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.
- NP715448.RAtij1mtLcSXwv28p8oZWpPFg4eLVDxnzKLCIZ3MECGfU130_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." NP715448.RAtij1mtLcSXwv28p8oZWpPFg4eLVDxnzKLCIZ3MECGfU130_provenance.
- NP665435.RA0GXO6vR552UKZv_oZ2j1XjseoUrGC4inHWjiEP6aPJg130_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." NP665435.RA0GXO6vR552UKZv_oZ2j1XjseoUrGC4inHWjiEP6aPJg130_provenance.
- NP715447.RAIuJFQpOTq-qKnkCfwKG7gZJDRtwtyPyokXcQ7hJ-V2Y130_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." NP715447.RAIuJFQpOTq-qKnkCfwKG7gZJDRtwtyPyokXcQ7hJ-V2Y130_provenance.
- 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.