Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion type Assertion NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_head.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion wasGeneratedBy ECO_0000203 NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_provenance.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion wasDerivedFrom befree-20150227 NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_provenance.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion SIO_000772 18165683 NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_provenance.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion evidence source_evidence_literature NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_provenance.
- NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_assertion description "[KCNQ1 (Kv7.1), the founding subfamily member, encodes a channel subunit directly implicated in genetic disorders, such as the long QT syndrome, a cardiac pathology responsible for arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523150.RAOGy3FXEFyyfT9ckID_AI0H1DKfH5fN6gp2DZ559hceU130_provenance.