Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion type Assertion NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_head.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion description "[Large deletion in KCNQ1 identified in a family with Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_provenance.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion evidence source_evidence_literature NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_provenance.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion SIO_000772 25187895 NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_provenance.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion wasDerivedFrom befree-2016 NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_provenance.
- NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_assertion wasGeneratedBy ECO_0000203 NP1216726.RAaaMaXrKG5LHJ2jselSybtsuz2UsRoODU3PEoEnhOCSE130_provenance.