Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion> ?p ?o ?g. }
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- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion type Assertion NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_head.
- 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.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion evidence source_evidence_literature NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion SIO_000772 19155175 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion wasDerivedFrom befree-20150227 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion wasGeneratedBy ECO_0000203 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.