Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion> ?p ?o ?g. }
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- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion type Assertion NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_head.
- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion description "[We identified a Syrian family with two children of consanguineous parents from two branches affected with congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion evidence source_evidence_literature NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion SIO_000772 24938146 NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion wasDerivedFrom befree-20150227 NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_assertion wasGeneratedBy ECO_0000203 NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.