Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion type Assertion NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_head.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion evidence source_evidence_literature NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion SIO_000772 24101679 NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion wasDerivedFrom befree-2016 NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion wasGeneratedBy ECO_0000203 NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.