Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion> ?p ?o ?g. }
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- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion type Assertion NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_head.
- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion description "[LMNA mutations represent the most prevalent genetic DCM cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_provenance.
- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion evidence source_evidence_literature NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_provenance.
- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion SIO_000772 21846512 NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_provenance.
- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion wasDerivedFrom befree-2016 NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_provenance.
- NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_assertion wasGeneratedBy ECO_0000203 NP917403.RAOlGjcRMudxOPH0LsrZBqzXZs-J99Dz3qpP43RpaXqBs130_provenance.