Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion> ?p ?o ?g. }
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- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion type Assertion NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_head.
- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion description "[Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_provenance.
- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion evidence source_evidence_literature NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_provenance.
- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion SIO_000772 23404334 NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_provenance.
- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion wasDerivedFrom befree-20150227 NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_provenance.
- NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_assertion wasGeneratedBy ECO_0000203 NP834893.RAxUvqZ7i-GVo7nR5ralJeuN6HzvmxfS4HT2Aq0Dh7hn0130_provenance.