Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion evidence source_evidence_literature NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion SIO_000772 23404334 NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion wasDerivedFrom befree-20140225 NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion wasGeneratedBy ECO_0000203 NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.