Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion> ?p ?o ?g. }
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- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion type Assertion NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_head.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion description "[These data matched the clinical observations on patients with SCN5A loss-of-function mutations with either severe or mild conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion evidence source_evidence_literature NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion SIO_000772 20174578 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion wasDerivedFrom befree-20140225 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion wasGeneratedBy ECO_0000203 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.