Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion> ?p ?o ?g. }
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- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion type Assertion NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_head.
- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion description "[Mutations in troponin T (TNNT2) gene represent the important part of currently identified disease-causing mutations in hypertrophic (HCM) and dilated (DCM) cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion evidence source_evidence_literature NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion SIO_000772 22292720 NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion wasDerivedFrom befree-20150227 NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_assertion wasGeneratedBy ECO_0000203 NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.