Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion> ?p ?o ?g. }
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- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion type Assertion NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_head.
- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion description "[To test this hypothesis, we performed case-control analyses on all DNA polymorphic variation identified in a resequencing study of six candidate DCM genes (CSRP3, LDB3, MYH7, SCN5A, TCAP, and TNNT2) conducted in 289 unrelated white probands with DCM of unknown cause and 188 unrelated white controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_provenance.
- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion evidence source_evidence_literature NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_provenance.
- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion SIO_000772 20201937 NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_provenance.
- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion wasDerivedFrom gad-20150221 NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_provenance.
- NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_assertion wasGeneratedBy ECO_0000203 NP166612.RAn5o2XqMhim-mzltpvKPPtisAHS9z-_6OiPakB27PbsI130_provenance.