Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP748717.RA0uGAYwOTHdeuuwYfQbi2HqXDtjS669a9TlVQTIJ18eU130_provenance.