Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_assertion description "[We describe a severe congenital myasthenic syndrome (CMS) caused by two missense mutations in the gene encoding the muscle specific receptor tyrosine kinase (MUSK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_assertion evidence source_evidence_literature NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_assertion SIO_000772 20371544 NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_assertion wasDerivedFrom befree-20140225 NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_assertion wasGeneratedBy ECO_0000203 NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP568201.RAt_mB5Jg6ARqW1yDVVwfHECDhhmvhw3QwFsI3nU5NACw130_provenance.