Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_assertion description "[This region also contains a locus for right ventricular cardiomyopathy (ARVD5) and the cardiac sodium channel gene (SCN5A), mutations that cause isolated progressive cardiac conduction defect (Lenegre syndrome), long-QT syndrome (LQT3), and Brugada syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_assertion evidence source_evidence_literature NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_assertion SIO_000772 15466643 NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_assertion wasDerivedFrom befree-20150227 NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_assertion wasGeneratedBy ECO_0000203 NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683219.RAjcCA04FdQkwqoJeNUe71CjXWcgRU6x1WELB7hK2VGHM130_provenance.