Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion> ?p ?o ?g. }
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- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion type Assertion NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_head.
- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.
- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion evidence source_evidence_literature NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.
- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion SIO_000772 18479388 NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.
- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion wasDerivedFrom lhgdn-20090331 NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.
- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion wasGeneratedBy ECO_0000203 NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.