Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion type Assertion NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_head.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion evidence source_evidence_literature NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion SIO_000772 19412328 NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion wasDerivedFrom gad-20150221 NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion wasGeneratedBy ECO_0000203 NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.