Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_assertion description "[Cx40 is abundant in the atrium, and homozygosity for the linked polymorphisms combined with an SCN5A mutation appeared to be responsible for familial atrial standstill.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_assertion evidence source_evidence_literature NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_assertion SIO_000772 16646598 NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_assertion wasDerivedFrom befree-20150227 NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_assertion wasGeneratedBy ECO_0000203 NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP425873.RAIc5liwn4SnzBatBQoBkQySufeARuQk6oT3ps-H8nrQ8130_provenance.