Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion> ?p ?o ?g. }
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- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion type Assertion NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_head.
- 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.
- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion evidence source_evidence_literature NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_provenance.
- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion SIO_000772 19155175 NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_provenance.
- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion wasDerivedFrom befree-20140225 NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_provenance.
- NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_assertion wasGeneratedBy ECO_0000203 NP399187.RATsMDFtQzugcB2STVkeLwdzkbXt5Y115E9TwvtySy3zQ130_provenance.