Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP220672.RA10StxZvLh_TBjxyuFfOHYNFvPnpLQjX6D_KPv5AZHus130_provenance.