Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion> ?p ?o ?g. }
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- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion type Assertion NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_head.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_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." NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion evidence source_evidence_literature NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion SIO_000772 19412328 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion wasDerivedFrom gad-20130706 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion wasGeneratedBy ECO_0000203 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.